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Medical Devices

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November 2001 510(k) Clearances

SUBMITTER ADDRESS LISTING FOR CDRH SUBSTANTIALLY EQUIVALENT (SE)
          510(K) SUMMARIES OR 510(K) STATEMENTS FOR FINAL
DECISIONS RENDERED DURING THE PERIOD 01-NOV-2001 THROUGH 30-NOV-2001

 
DEVICE: SF SH CATHETER, MODEL R65-945
A & A MEDICAL, INC.               510(k) NO: K013437(TRADITIONAL)
ATTN: JAY  MANSOUR                PHONE NO : 770-343-8400
9370 INDUSTRIAL TRACE             SE DECISION MADE: 19-NOV-01
ALPHARETTA, GA 30004-3383         510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: HSG CATHETER SET, 5F MODEL RGS0947, HSG CATHETER SET, 7F, MODEL
A & A MEDICAL, INC.               510(k) NO: K013491(TRADITIONAL)
ATTN: JAY  MANSOUR                PHONE NO : 770-343-8400
9370 INDUSTRIAL TRACE             SE DECISION MADE: 19-NOV-01
ALPHARETTA, GA 30004-3383         510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: HEPARIN COATED MINIATURE CENTRIFUGAL BYPASS PUMP SYSTEM;MODEL #C
A-MED SYSTEMS, INC.               510(k) NO: K013393(SPECIAL)
ATTN: CYNTHIA G ROYSTER           PHONE NO : 916-375-7400
2491 BOATMAN AVE.                 SE DECISION MADE: 09-NOV-01
WEST SACRAMENTO, CA 95691         510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: ACON BAR ONE STEP BARBITURATES TEST STRIP, ACON BAR ONE STEP BAR
ACON LABORATORIES, INC.           510(k) NO: K012824(TRADITIONAL)
ATTN: EDWARD  TUNG                PHONE NO : 858-535-2030
4108 SORRENTO VALLEY BLVD.        SE DECISION MADE: 09-NOV-01
SAN DIEGO, CA 92121               510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: ACRYDERM SILVER ANTTIMICROBIAL WOUND GEL MODEL# A-002101
ACRYMED, INC.                     510(k) NO: K011994(TRADITIONAL)
ATTN: BRUCE  GIBBINS              PHONE NO : 503-624-9830
12232 SW GARDEN PLACE             SE DECISION MADE: 08-NOV-01
PORTLAND, OR 97223                510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: CONGRUENT BONE PLATE SYSTEM
ACUMED, INC.                      510(k) NO: K012655(TRADITIONAL)
ATTN: SHARI  JEFFERS              PHONE NO : 503-627-9957
10950 S.W. 5TH ST., SUITE 170     SE DECISION MADE: 07-NOV-01
BEAVERTON, OR 97005               510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: MODIFICATION TO SKYLIGHT IMAGING SYSTEM
ADAC LABORATORIES                 510(k) NO: K013496(TRADITIONAL)
ATTN: DAVID  KOLESAR              PHONE NO : 408-468-3455
540 ALDER DR.                     SE DECISION MADE: 06-NOV-01
MILPITAS, CA 95035                510(k) SUMMARY AVAILABLE FROM FDA
                                  THIRD PARTY REVIEW

DEVICE: GEMINI IMAGING SYSTEM
ADAC LABORATORIES                 510(k) NO: K013521(TRADITIONAL)
ATTN: COLEEN A COLEMAN            PHONE NO : 408-468-3051
540 ALDER DR.                     SE DECISION MADE: 07-NOV-01
MILPITAS, CA 95035                510(k) SUMMARY AVAILABLE FROM FDA
                                  THIRD PARTY REVIEW

DEVICE: ALTAIR MODEL, DEI SYSTEM (DIFFRACTIVE ENERGY IMAGING SYSTEM)
ADVANCED DIAGNOSTICS, INC.        510(k) NO: K013291(TRADITIONAL)
ATTN: STEVE  HESLER               PHONE NO : 425-222-7169
8112 304TH AVE. SE                SE DECISION MADE: 14-NOV-01
PRESTON, WA 98050                 510(k) SUMMARY AVAILABLE FROM FDA

 
DEVICE: MACS HMA ANTERIOR SPINAL STABILIZATION SYSTEM
AESCULAP, INC.                    510(k) NO: K011556(TRADITIONAL)
ATTN: LISA M MILLINGTON           PHONE NO : 610-791-6882
3773 CORPORATE PKWY.              SE DECISION MADE: 16-NOV-01
CENTER VALLEY, PA 18034           510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: ADC PEDIATRIC
AGFA CORP.                        510(k) NO: K012750(TRADITIONAL)
ATTN: T. WHIT  ATHEY              PHONE NO : 301-770-9590
12300 TWINBROOK PKWY,STE 625      SE DECISION MADE: 14-NOV-01
ROCKVILLE, MD 20852               510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: DRYSTAR, MODEL 4500M
AGFA CORP.                        510(k) NO: K012941(TRADITIONAL)
ATTN: T. WHIT  ATHEY              PHONE NO : 301-770-9590
12300 TWINBROOK PKWY,STE 625      SE DECISION MADE: 29-NOV-01
ROCKVILLE, MD 20852               510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: SINGLE DOSE DISPENSING PIN, MODEL 2201
ALARIS MEDICAL SYSTEMS, INC.      510(k) NO: K013087(TRADITIONAL)
ATTN: RENEE L FLUET               PHONE NO : 858-458-7563
10221 WATERIDGE CIR.              SE DECISION MADE: 13-NOV-01
SAN DIEGO, CA 92121-2733          510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: TST CONTROL INTEGRATOR FOR STEAM STERILIZERS
ALBERT BROWNE LTD.                510(k) NO: K002937(TRADITIONAL)
ATTN: CYNTHIA J.M.  NOLTE         PHONE NO : 508-643-0434
49 PLAIN STREET                   SE DECISION MADE: 05-NOV-01
NORTH ATTLEBORO, MA 02760         510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: COMPRESSIBLE LIMB SLEEVE
ALLIANCE MEDICAL CORP.            510(k) NO: K011192(TRADITIONAL)
ATTN: DON  SELVEY                 PHONE NO : 480-763-5300
10232 SOUTH 51ST STREET           SE DECISION MADE: 26-NOV-01
PHOENIX, AZ 85044                 510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: REPROCESSED AUTOSUTURE UNIPOLAR LAPAROSCOPIC/ENDOSCOPIC INSTRUME
ALLIANCE MEDICAL CORP.            510(k) NO: K012603(TRADITIONAL)
ATTN: DON  SELVEY                 PHONE NO : 480-763-5300
10232 SOUTH 51ST. STREET          SE DECISION MADE: 07-NOV-01
PHOENIX, AZ 85044                 510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: REPROCESSED ATHROSCOPICS BURS
ALLIANCE MEDICAL CORP.            510(k) NO: K012605(TRADITIONAL)
ATTN: DON  SELVEY                 PHONE NO : 480-763-5300
10232 SOUTH 51ST. STREET          SE DECISION MADE: 07-NOV-01
PHOENIX, AZ 85044                 510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: REPROCESSED STRYKER ARTHROSCOPIC SHAVERS
ALLIANCE MEDICAL CORP.            510(k) NO: K012635(TRADITIONAL)
ATTN: DON  SELVEY                 PHONE NO : 480-763-5300
10232 SOUTH 51ST ST.              SE DECISION MADE: 07-NOV-01
PHOENIX, AZ 85044                 510(k) SUMMARY AVAILABLE FROM FDA

 
DEVICE: REPROCESSED LAPAROSCOPIC/ENDOSCOPIC INSTRUMENTS
ALLIANCE MEDICAL CORP.            510(k) NO: K012638(TRADITIONAL)
ATTN: DON  SELVEY                 PHONE NO : 480-763-5300
10232 SOUTH 51ST ST.              SE DECISION MADE: 08-NOV-01
PHOENIX, AZ 85044                 510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: REPROCESSED DYONICS ARTHROSCOPIC BURS
ALLIANCE MEDICAL CORP.            510(k) NO: K012652(TRADITIONAL)
ATTN: DON  SELVEY                 PHONE NO : 480-763-5300
10232 SOUTH 51ST. STREET          SE DECISION MADE: 08-NOV-01
PHOENIX, AZ 85044                 510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: REPROCESSED DYONICS ARTHROSCOPIC SHAVERS
ALLIANCE MEDICAL, INC.            510(k) NO: K012611(TRADITIONAL)
ATTN: DON  SELVEY                 PHONE NO : 480-763-5300
10232 SOUTH 51 STREET             SE DECISION MADE: 07-NOV-01
PHOENIX, AZ 85044                 510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: REPROCSSED LINVATEC SHAVERS
ALLIANCE MEDICAL, INC.            510(k) NO: K012613(TRADITIONAL)
ATTN: DON  SELVEY                 PHONE NO : 480-763-5300
10232 SOUTH 51 STREET             SE DECISION MADE: 07-NOV-01
PHOENIX, AZ 85044                 510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: REPROCESSED LINVATEC ARTHROSCOPIC BURS
ALLIANCE MEDICAL, INC.            510(k) NO: K012630(TRADITIONAL)
ATTN: DON  SELVEY                 PHONE NO : 480-763-5300
10232 SOUTH 51 STREET             SE DECISION MADE: 09-NOV-01
PHOENIX, AZ 85044                 510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: REPROCESSED PHACOEMULSIFICATION TIPS
ALLIANCE MEDICAL, INC.            510(k) NO: K012637(TRADITIONAL)
ATTN: DON  SELVEY                 PHONE NO : 480-763-5300
10232 SOUTH 51 STREET             SE DECISION MADE: 07-NOV-01
PHOENIX, AZ 85044                 510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: AMEDITECH IMMUTEST DRUG SCREEN OPIATES
AMEDITECH, INC.                   510(k) NO: K012483(TRADITIONAL)
ATTN: JOHN  WU                    PHONE NO : 858-535-1968
10340 CAMINO SANTA FE, STE F      SE DECISION MADE: 30-NOV-01
SAN DIEGO, CA 92121               510(k) STATEMENT

DEVICE: AMEDITECH IMMUTEST DRUG SCREEN AMPHETAMINE
AMEDITECH, INC.                   510(k) NO: K012484(TRADITIONAL)
ATTN: JOHN  WU                    PHONE NO : 858-535-1968
10340 CAMINO SANTA FE, STE F      SE DECISION MADE: 30-NOV-01
SAN DIEGO, CA 92121               510(k) STATEMENT

DEVICE: AMEDITECH IMMUTEST DRUG SCREEN PCP
AMEDITECH, INC.                   510(k) NO: K012582(TRADITIONAL)
ATTN: JOHN  WU                    PHONE NO : 858-535-1968
10340 CAMINO SANTA FE, STE F      SE DECISION MADE: 30-NOV-01
SAN DIEGO, CA 92121               510(k) STATEMENT

 
DEVICE: AMEDITECH IMMUTEST DRUG SCREEN METHAMPHETAMINE
AMEDITECH, INC.                   510(k) NO: K012585(TRADITIONAL)
ATTN: JOHN  WU                    PHONE NO : 858-535-1968
10340 CAMINO SANTA FE, STE F      SE DECISION MADE: 16-NOV-01
SAN DIEGO, CA 92121               510(k) STATEMENT

DEVICE: 'RAPIDONE'-METHADONE TEST
AMERICAN BIO MEDICA CORP.         510(k) NO: K012164(TRADITIONAL)
ATTN: HENRY  WELLS                PHONE NO : 410-992-4734
9110 RED BRANCH ROAD              SE DECISION MADE: 20-NOV-01
COLUMBIA, MD 21945                510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: RAPIDONE-ECSTASY TEST
AMERICAN BIO MEDICA CORP.         510(k) NO: K013180(TRADITIONAL)
ATTN: HENRY  WELLS                PHONE NO : 410-992-4734
9110 RED BRANCH ROAD              SE DECISION MADE: 26-NOV-01
COLUMBIA, MD 21045                510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: ADC 656 ELECTRONIC STETHOSCOPE
AMERICAN DIAGNOSTIC CORP.         510(k) NO: K012304(TRADITIONAL)
ATTN: MARC  BLITSTEIN             PHONE NO : 516-273-9600
55 COMMERCE DR.                   SE DECISION MADE: 01-NOV-01
HAUPPAUGE, NY 11788               510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: MODIFICATION TO:MICRO TOUCH (R) POWDER FREE LATEX SURGICAL GLOVE
ANSELL HEALTHCARE PRODUCTS, INC.  510(k) NO: K013603(SPECIAL)
ATTN: JAMES R CHATTERTON          PHONE NO : 330-833-2811
1875 HARSH AVENUE, SE             SE DECISION MADE: 13-NOV-01
MASSILLON, OH 44646               510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: MODIFICATION TO: ULTRALON (R) POWDER FREE LATEX SURGICAL GLOVES
ANSELL HEALTHCARE PRODUCTS, INC.  510(k) NO: K013604(SPECIAL)
ATTN: JAMES R CHATTERTON          PHONE NO : 330-833-2811
1875 HARSH AVENUE, SE             SE DECISION MADE: 13-NOV-01
MASSILLON, OH 44646               510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: APEX MODULAR ALUMINA FEMORAL HEAD
APEX SURGICAL, LLC.               510(k) NO: K012918(TRADITIONAL)
ATTN: EDWARD J CHEAL              PHONE NO : 508-947-6500
12 HARDING STREET,SUITE 202       SE DECISION MADE: 27-NOV-01
LAKEVILLE, MA 02347               510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: SURESET INFUSION SET, MODEL 8023
APPLIED DIABETES RESEARCH, INCORPO510(k) NO: K012429(TRADITIONAL)
ATTN: CHARLES H KYPER             PHONE NO :
103 NOLEN LANE                    SE DECISION MADE: 06-NOV-01
CHAPEL HILL, NC 27516             510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: ARTHROCARE ARTHRO WANDS, ENETEC EVAC PLASMA WAND
ARTHROCARE CORP.                  510(k) NO: K013463(SPECIAL)
ATTN: BRUCE  PROTHRO              PHONE NO : 408-736-0224
595 NORTH PASTORIA AVE.           SE DECISION MADE: 15-NOV-01
SUNNYVALE, CA 94085-2936          510(k) SUMMARY AVAILABLE FROM FDA

 
DEVICE: RESORBABLE SCREW ANCHOR
ARTHROTEK, INC.                   510(k) NO: K012872(TRADITIONAL)
ATTN: SARA B SHULTZ               PHONE NO : 219-267-6639
56 EAST BELLE DRIVE               SE DECISION MADE: 20-NOV-01
P.O. BOX 587                      510(k) SUMMARY AVAILABLE FROM FDA
WARSAW, IN 46582

DEVICE: ASTRA TECH IMPLANTS-DENTAL SYSTEM
ASTRA TECH, INC.                  510(k) NO: K012965(TRADITIONAL)
ATTN: BRUCE R MANNING             PHONE NO : 508-393-3100
96 WEST MAIN STREET               SE DECISION MADE: 19-NOV-01
NORTHBOROUGH, MA 01532            510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: MODIFICATION TO BASIC DENTAL IMPLANT SYSTEM
BASIC DENTAL IMPLANT SYSTEMS, INC.510(k) NO: K013682(SPECIAL)
ATTN: DAN  BLACKLOCK              PHONE NO : 505-881-1376
3321 COLUMBIA, N.E.               SE DECISION MADE: 28-NOV-01
ALBUQUERQUE, NM 87107-2001        510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: RENU MULTIPLUS NO RUB MULTI-PURPOSE SOLUTION
BAUSCH & LOMB, INC.               510(k) NO: K011796(TRADITIONAL)
ATTN: PAUL G STAPLETON            PHONE NO : 716-338-8172
1400 NORTH GOODMAN ST.            SE DECISION MADE: 01-NOV-01
ROCHESTER, NY 14603               510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: DOCUMENTING LASER SLIT LAMP, DP 2010
BAUSCH & LOMB, INC.               510(k) NO: K012873(TRADITIONAL)
ATTN: PENNI L PANNELL             PHONE NO : 949-454-4530
9342 JERONIMO RD.                 SE DECISION MADE: 19-NOV-01
IRVINE, CA 92718                  510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: CYBERCASES BY BAUSCH & LOMB
BAUSCH & LOMB, INC.               510(k) NO: K013232(TRADITIONAL)
ATTN: KIM S DEVITTO               PHONE NO : 716-338-6401
1400 NORTH GOODMAN ST.            SE DECISION MADE: 20-NOV-01
P.O. BOX 30450                    510(k) SUMMARY AVAILABLE FROM FDA
ROCHESTER, NY 14603-0450

DEVICE: ADVIA 1650 GLUCOSE HEXOKINASE 11 ASSAY
BAYER CORP.                       510(k) NO: K011963(TRADITIONAL)
ATTN: KENNETH T EDDS              PHONE NO : 914-524-2446
511 BENEDICT AVE.                 SE DECISION MADE: 20-NOV-01
TARRYTOWN, NY 10591-5097          510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: INSYTE, ANGIOCATH, INSYTE AUTOGUARD, ANGIOCATH AUTOGUARD, AUTOGU
BECTON DICKINSON INFUSION THERAPY 510(k) NO: K013073(TRADITIONAL)
ATTN: LESLIE  WOOD                PHONE NO : 801-565-2504
9450 SOUTH STATE ST.              SE DECISION MADE: 08-NOV-01
SANDY, UT 84070                   510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: ICE BATON
BEHIVE LTD                        510(k) NO: K012746(TRADITIONAL)
ATTN: MARY  MCNAMARA-CULLINANE    PHONE NO : 508-643-0434
49 PLAIN STREET                   SE DECISION MADE: 14-NOV-01
NORTH ATTLEBORO, MA 02760         510(k) SUMMARY AVAILABLE FROM FDA

 
DEVICE: MED-RX IRRIGATION SET, MODEL 10-3001, 10-3002, 10-4000, 10-4001
BENLAN, INC.                      510(k) NO: K010607(TRADITIONAL)
ATTN: BILL  LIM                   PHONE NO : 905 829 5004
2760 BRIGHTON RD.                 SE DECISION MADE: 28-NOV-01
OAKVILLE, ONTARIO, CANADA L6H 5T4 510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: BINAX NOW STREPTOCOCCUS PNEUMONIAE TEST
BINAX, INC.                       510(k) NO: K012521(TRADITIONAL)
ATTN: PAMELA  ANGELL              PHONE NO : 207-772-3988
217 READ ST.                      SE DECISION MADE: 30-NOV-01
PORTLAND, ME 04103                510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: STRIPMAX 1210 URINE CHEMISTRY ANALYZER, URIMATE REAGENT STRIP FO
BIOCARE CORP.                     510(k) NO: K012829(TRADITIONAL)
ATTN: BRUCE A MACFARLAND          PHONE NO : 952-646-3188
5182 WEST 76TH STREET             SE DECISION MADE: 02-NOV-01
MINNEAPOLIS, MN 55439             510(k) STATEMENT

DEVICE: INTEX SCREW
BIOMET, INC.                      510(k) NO: K012798(TRADITIONAL)
ATTN: DALENE T BINKLEY            PHONE NO : 800-348-9500
P.O. BOX 587                      SE DECISION MADE: 16-NOV-01
WARSAW, IN 46581-0587             510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: CARDIO CARE EKG-2000 12-CHANNEL ELECTROCARDIOGRAPH
BIONET COMPANY LTD                510(k) NO: K011328(TRADITIONAL)
ATTN: MIN SOO  HAN                PHONE NO : 822 346 83660
3F, DAEYANG BLDG., 999            SE DECISION MADE: 21-NOV-01
DAECHI-DONG, KANGNAM-GU           510(k) SUMMARY AVAILABLE FROM FDA
SEOUL, REPUBLIC OF KOREA

DEVICE: MODIFICATION TO: 1.5 BONE FIXATION KIT, MODELS BXS6114, BXS6214
BIONX IMPLANTS, INC.              510(k) NO: K013546(SPECIAL)
ATTN: TUIJA  ANNALA               PHONE NO : 358 331 65600
HERMIANKATU 6-8 L                 SE DECISION MADE: 21-NOV-01
TAMPERE, FINLAND FIN-33720        510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: BIOPLATE RESORBABLE BONE SCREW
BIOPLATE, INC.                    510(k) NO: K012908(TRADITIONAL)
ATTN: ERIC V HOHENSTEIN           PHONE NO : 323-549-9500
6911 MELROSE AVE.                 SE DECISION MADE: 28-NOV-01
LOS ANGELES, CA 90038             510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: THE BIOPLATE MANDIBLE FIXATION SYSTEM
BIOPLATE, INC.                    510(k) NO: K012910(TRADITIONAL)
ATTN: BRUCE F MACKLER             PHONE NO : 202-912-2000
1666 K STREET NW                  SE DECISION MADE: 20-NOV-01
SUITE 200                         510(k) STATEMENT
WASHINGTON, DC 20006-4004

DEVICE: CARTO XP EP NAVIGATION SYSTEM
BIOSENSE WEBSTER, INC.            510(k) NO: K013083(SPECIAL)
ATTN: AMY  WALTERS                PHONE NO : 909-839-8804
3333 DIAMOND CANYON RD.           SE DECISION MADE: 21-NOV-01
DIAMOND BAR, CA 91765             510(k) SUMMARY AVAILABLE FROM FDA

 
DEVICE: ULTRA-THIN SDS BALLOON DILATATION CATHETER
BOSTON SCIENTIFIC CORP.           510(k) NO: K011909(TRADITIONAL)
ATTN: JENNIFER  BOLTON            PHONE NO : 508-652-5972
ONE BOSTON SCIENTIFIC PLACE       SE DECISION MADE: 28-NOV-01
NATICK, MA 01760                  510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: WALLSTENT RX BILIARY ENDOPROSTHESES, MODELS 6961-6972 INCLUSIVE
BOSTON SCIENTIFIC CORP.           510(k) NO: K012752(TRADITIONAL)
ATTN: KATHLEEN  MORAHAN           PHONE NO : 508-652-5942
ONE BOSTON SCIENTIFIC PL.         SE DECISION MADE: 15-NOV-01
NATICK, MA 01760-1537             510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: MODIFICATION TO SCOOPER DRUG/ADULTERATION TEST CUP
BRANAN MEDICAL CORP.              510(k) NO: K013124(SPECIAL)
ATTN: RAPHAEL  WONG               PHONE NO : 949-598-7166
10015 MUIRLANDS RD., SUITE E      SE DECISION MADE: 07-NOV-01
IRVINE, CA 92618                  510(k) STATEMENT

DEVICE: MODIFICATION TO HEARTWAVE ALTERNANS PROCESSING SYSTEM, MODEL APS
CAMBRIDGE HEART, INC.             510(k) NO: K013564(SPECIAL)
ATTN: JOHN  GREENBAUM             PHONE NO : 954-680-2548
20310 SW 48TH ST.                 SE DECISION MADE: 21-NOV-01
FT. LAUDERDALE, FL 33332          510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: CARDIAC DIAGNOSTIC SYSTEM, MODEL CH2000
CAMBRIDGE HEART, INC.             510(k) NO: K013565(SPECIAL)
ATTN: JOHN  GREENBAUM             PHONE NO : 954-680-2548
20310 SW 48TH ST.                 SE DECISION MADE: 21-NOV-01
FT. LAUDERDALE, FL 33332          510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: POWERHEART CARDIAC RHYTHM MODULE
CARDIAC SCIENCE, INC.             510(k) NO: K012197(TRADITIONAL)
ATTN: SEW-WAH  TAY                PHONE NO : 952-939-2942
5420 FELTL ROAD                   SE DECISION MADE: 16-NOV-01
MINNEAPOLIS, MN 55343             510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: MODIFICATION TO BIOZ.COM HEMODYNAMIC MONITOR
CARDIODYNAMICS INTERNATIONAL CORP.510(k) NO: K011439(TRADITIONAL)
ATTN: BRIAN  PARK                 PHONE NO : 858-535-0202
6175 NANCY RIDGE DR., #300        SE DECISION MADE: 02-NOV-01
SAN DIEGO, CA 92121               510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: BERNOULLI VENTILATOR MANAGEMENT SYSTEM
CARDIOPULMONARY CORP.             510(k) NO: K011861(TRADITIONAL)
ATTN: JOHN  LAVIOLA               PHONE NO : 203-877-1999
200 CASCADE BLVD.                 SE DECISION MADE: 06-NOV-01
MILFORD, CT 06460                 510(k) STATEMENT

DEVICE: VISULAS 532S
CARL ZEISS, INC.                  510(k) NO: K013402(SPECIAL)
ATTN: KENNETH M NICOLL            PHONE NO : 914-747-1800
ONE ZEISS DR.                     SE DECISION MADE: 14-NOV-01
THORNWOOD, NY 10594               510(k) SUMMARY AVAILABLE FROM FDA

 
DEVICE: TOTAL O2
CHAD THERAPEUTICS, INC.           510(k) NO: K013472(TRADITIONAL)
ATTN: KEVIN  MCCULLOH             PHONE NO : 818-882-0883
21622 PLUMMER ST.                 SE DECISION MADE: 28-NOV-01
CHATSWORTH, CA 91311              510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: DUR-8, MODELS DUR-8
CIRCON VIDEO                      510(k) NO: K012925(TRADITIONAL)
ATTN: WAYNE  STERNER              PHONE NO : 805-685-5100
6500 HOLLISTER AVE.               SE DECISION MADE: 07-NOV-01
SANTA BARBARA, CA 93117           510(k) STATEMENT

DEVICE: FLEXIBLE PEDIATRIC CYSTOURETEROSCOPE, MODEL AUR- 735
CIRCON VIDEO                      510(k) NO: K012929(TRADITIONAL)
ATTN: WAYNE  STERNER              PHONE NO : 805-685-5100
6500 HOLLISTER AVE.               SE DECISION MADE: 19-NOV-01
SANTA BARBARA, CA 93117           510(k) STATEMENT

DEVICE: APN-2 USA SERIES FLEXIBLE CHOLEDOCHOSCOPE
CIRCON VIDEO                      510(k) NO: K012951(TRADITIONAL)
ATTN: WAYNE B STERNER             PHONE NO : 805-685-5100
6500 HOLLISTER AVE.               SE DECISION MADE: 09-NOV-01
SANTA BARBARA, CA 93117           510(k) STATEMENT

DEVICE: THE V BAG, CATALOG NUMBER VB1800; VAC-BOX FOR VACUUM ASSISTED VE
CIRCULATORY TECHNOLOGY, INC.      510(k) NO: K012942(TRADITIONAL)
ATTN: YEHUDA  TAMARI              PHONE NO : 516-624-2424
21 SINGWORTH ST.                  SE DECISION MADE: 05-NOV-01
OYSTER BAY, NY 11771              510(k) STATEMENT

DEVICE: LINICAL PROTEIN I CALIBRATION VERIFIERS LEVELS A=E FOR BECKMAN C
CLINIQA CORPORATION               510(k) NO: K013332(TRADITIONAL)
ATTN: CAROL  RUGGIERO             PHONE NO : 760-744-1900
1432-B SOUTH MISSION ROAD         SE DECISION MADE: 20-NOV-01
FALLBROOK, CA 92028               510(k) STATEMENT

DEVICE: SORIN BIOMEDICA SMART BCD VANGUARD,SURFACE MODIFIED BLOOD CARDIO
COBE CARDIOVASCULAR, INC.         510(k) NO: K012763(ABBREVIATED)
ATTN: LYNNE  LEONARD              PHONE NO : 303-467-6586
14401 WEST 65TH WAY               SE DECISION MADE: 15-NOV-01
ARVADA, CO 80004                  510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: COBE SMARXT OPTIMIN SURFACE MODIFIED HOLLOW FIBER MEMBRANE OXYGE
COBE CARDIOVASCULAR, INC.         510(k) NO: K013480(SPECIAL)
ATTN: SHAWN  RIEDEL               PHONE NO : 303-467-6521
14401 WEST 65TH WAY               SE DECISION MADE: 16-NOV-01
ARVADA, CO 80004                  510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: FANELLI BILIARY STENT
COOK, INC.                        510(k) NO: K010601(TRADITIONAL)
ATTN: LISA  HOPKINS               PHONE NO : 812-339-2235
925 SOUTH CURRY PIKE              SE DECISION MADE: 16-NOV-01
P.O. BOX 489                      510(k) SUMMARY AVAILABLE FROM FDA
BLOOMINGTON, IN 47402

 
DEVICE: SPECTRUM VENTRICULAR CATHETER
COOK, INC.                        510(k) NO: K011812(TRADITIONAL)
ATTN: APRIL  LAVENDER             PHONE NO : 812-339-2235
925 SOUTH CURRY PIKE              SE DECISION MADE: 08-NOV-01
P.O. BOX 489                      510(k) SUMMARY AVAILABLE FROM FDA
BLOOMINGTON, IN 47402

DEVICE: CORDIS AVIATOR PERIPHERAL DILATATION CATHETER
CORDIS, A JOHNSON & JOHNSON CO.   510(k) NO: K013581(SPECIAL)
ATTN: CHUCK  RYAN                 PHONE NO : 908-412-7446
7 POWDER HORN DRIVE               SE DECISION MADE: 28-NOV-01
WARREN, NJ 07059                  510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: DEEP GRAY
CORTECHS LLC                      510(k) NO: K012563(ABBREVIATED)
ATTN: JEFFREY M ANDERS            PHONE NO : 617-241-9588
6 13TH ST.                        SE DECISION MADE: 02-NOV-01
CHARLESTOWN, MA 02129-2027        510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: MONO-DOX, SYNTHETIC ABSORBABLE POLYDIOXANONE SURGICAL SUTURE,STE
CP MEDICAL                        510(k) NO: K013274(TRADITIONAL)
ATTN: MARY ANN  GREENAWALT        PHONE NO : 503-232-1555
836 N.E. 24TH AVE.                SE DECISION MADE: 16-NOV-01
PORTLAND, OR 97232                510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: CYNOSURE PHOTOGENICA ER
CYNOSURE, INC.                    510(k) NO: K012790(TRADITIONAL)
ATTN: GEORGE  CHO                 PHONE NO : 978-256-4200
10 ELIZABETH DR.                  SE DECISION MADE: 16-NOV-01
CHELMSFORD, MA 01824              510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: CYNOSURE PHOTOGENICA VL
CYNOSURE, INC.                    510(k) NO: K012806(TRADITIONAL)
ATTN: GEORGE  CHO                 PHONE NO : 978-256-4200
10 ELIZABETH DR.                  SE DECISION MADE: 19-NOV-01
CHELMSFORD, MA 01824              510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: DIMENSION HAIC ASSAY, MODEL DF105
DADE BEHRING, INC.                510(k) NO: K011852(TRADITIONAL)
ATTN: CATHY  CRAFT                PHONE NO : 302-631-6280
GLASGOW BUSINESS COMMUNITY        SE DECISION MADE: 15-NOV-01
P.O. BOX 6101, BUILDING 500       510(k) SUMMARY AVAILABLE FROM FDA
NEWARK, DE 19714

DEVICE: BCS SYSTEM
DADE BEHRING, INC.                510(k) NO: K013114(TRADITIONAL)
ATTN: REBECCA S AYASH             PHONE NO : 302-631-6276
GLASGOW SITE                      SE DECISION MADE: 09-NOV-01
P.O. BOX 6101                     510(k) SUMMARY AVAILABLE FROM FDA
NEWARK, DE 19714

DEVICE: N LP(A) STANDARD SY
DADE BEHRING, INC.                510(k) NO: K013126(TRADITIONAL)
ATTN: REBECCA S AYASH             PHONE NO : 302-631-6276
GLASGOW SITE                      SE DECISION MADE: 09-NOV-01
P.O. BOX 6101                     510(k) SUMMARY AVAILABLE FROM FDA
NEWARK, DE 19714

 
DEVICE: NEUROMOVE NM900
DAN MED, INC.                     510(k) NO: K012885(TRADITIONAL)
ATTN: THOMAS  SANDGAARD           PHONE NO : 800-495-6670
4 WEST DRY CREEK CIRCLE,          SE DECISION MADE: 08-NOV-01
SUITE 260                         510(k) STATEMENT
DENVER, CO 80120

DEVICE: MODIFICATION TO: DATASCOPE 8FR. POLYIMIDE ALT B IAB, 25CC, 34CC,
DATASCOPE CORP.                   510(k) NO: K013326(SPECIAL)
ATTN: JOANN  WOLF                 PHONE NO : 973-244-6123
15 LAW DR.                        SE DECISION MADE: 02-NOV-01
FAIRFIELD, NJ 07004-3206          510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: DATEX-OHMEDA S/5 DEVICE INTERFACING SOLUTION, N-DISXXXX
DATEX-OHMEDA                      510(k) NO: K012531(TRADITIONAL)
ATTN: JOEL  KENT                  PHONE NO : 781-449-8685
86 PILGRIM ROAD                   SE DECISION MADE: 02-NOV-01
NEEDHAM, MA 02492                 510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: NORAD, NOCTURNAL ORAL AIRWAY DILATOR APPLIANCE
DENNIS R. BAILEY, DDS             510(k) NO: K013049(TRADITIONAL)
ATTN: DENNIS R BAILEY             PHONE NO : 303-770-3300
7901 EAST BELLEVIEW AVENUE        SE DECISION MADE: 29-NOV-01
SUITE 200                         510(k) SUMMARY AVAILABLE FROM FDA
ENGLEWOOD, CO 80111

DEVICE: TULSA CONTRA ANGLES
DENTSPLY INTL.                    510(k) NO: K012720(TRADITIONAL)
ATTN: P. JEFFREY  LEHN            PHONE NO : 717-845-7511
570 WEST COLLEGE AVE              SE DECISION MADE: 08-NOV-01
YORK, PA 17404                    510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: SYMPHONY GRAFT DELIVERY SYSTEM (GDS)
DEPUY ACROMED                     510(k) NO: K012738(TRADITIONAL)
ATTN: KAREN F JURCZAK             PHONE NO : 508-828-3704
325 PARAMOUNT DR.                 SE DECISION MADE: 14-NOV-01
RAYNHAM, MA 02767                 510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: DISCOVERY FACET SCREW FIXATION SYSTEM
DEPUY ACROMED                     510(k) NO: K012773(TRADITIONAL)
ATTN: KAREN F JURCZAK             PHONE NO : 508-828-3704
325 PARAMOUNT DR.                 SE DECISION MADE: 16-NOV-01
RAYNHAM, MA 02767                 510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: SUMMIT OCCIPITO-CERVICO- THORACIC (OCT) SPINAL SYSTEM
DEPUY ACROMED                     510(k) NO: K013222(TRADITIONAL)
ATTN: KAREN F JURCZAK             PHONE NO : 508-828-3704
325 PARAMOUNT DR.                 SE DECISION MADE: 07-NOV-01
RAYNHAM, MA 02767                 510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: MODIFICATION TO: STACKABLE CAGE SYSTEM
DEPUY ACROMED                     510(k) NO: K013382(SPECIAL)
ATTN: KAREN F JURCZAK             PHONE NO : 508-828-3704
325 PARAMOUNT DR.                 SE DECISION MADE: 07-NOV-01
RAYNHAM, MA 02767                 510(k) SUMMARY AVAILABLE FROM FDA

 
DEVICE: ISOLA POLYAXIAL WASHER
DEPUY ACROMED                     510(k) NO: K013441(SPECIAL)
ATTN: LISA  GILMAN                PHONE NO : 508-828-8287
325 PARAMOUNT DR.                 SE DECISION MADE: 16-NOV-01
RAYNHAM, MA 02767                 510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: FRONTIER ANTERIOR SCOLIOSIS SYSTEM
DEPUY ACROMED, INC.               510(k) NO: K012916(TRADITIONAL)
ATTN: LISA  GILMAN                PHONE NO : 508-880-8287
325 PARAMOUNT DR.                 SE DECISION MADE: 27-NOV-01
RAYNHAM, MA 02767                 510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: BSM BONE SUBSTITUTE MATERIAL
DEPUY ORTHOPAEDICS, INC.          510(k) NO: K011048(TRADITIONAL)
ATTN: LYNNETTE  WHITAKER          PHONE NO : 219-371-4903
700 ORTHOPAEDIC DR.               SE DECISION MADE: 13-NOV-01
P.O. BOX 988                      510(k) SUMMARY AVAILABLE FROM FDA
WARSAW, IN 46581-0988

DEVICE: MODIFICATION TO DEPUY C-STEM SYSTEM
DEPUY ORTHOPAEDICS, INC.          510(k) NO: K013350(SPECIAL)
ATTN: MARCIA J ARENTZ             PHONE NO : 219-371-4944
700 ORTHOPAEDIC DR.               SE DECISION MADE: 07-NOV-01
WARSAW, IN 46581-0988             510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: MODIFICATION TO: STERILE COLLES CLASSIC FIXATOR
DEPUY ORTHOPAEDICS, INC.          510(k) NO: K013503(SPECIAL)
ATTN: MARCIA J ARENTZ             PHONE NO : 219-371-4944
700 ORTHOPAEDIC DR.               SE DECISION MADE: 16-NOV-01
WARSAW, IN 46581-0988             510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: IMMULITE INTACT PTH, IMMULITE 2000 INTACT PTH, MODELS LKPP1 (100
DIAGNOSTIC PRODUCTS CORP.         510(k) NO: K013566(SPECIAL)
ATTN: EDWARD M LEVINE             PHONE NO : 310-645-8200
5700 WEST 96TH ST.                SE DECISION MADE: 20-NOV-01
LOS ANGELES, CA 90045             510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: IRMA SL BLOOD ANALYSIS SYSTEM GL CARTRIDGE
DIAMETRICS MEDICAL, INC.          510(k) NO: K011586(TRADITIONAL)
ATTN: NANCY  RING                 PHONE NO : 651-639-8035
2658 PATTON RD.                   SE DECISION MADE: 16-NOV-01
ROSEVILLE, MN 55113               510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: DIOMED 15 PLUS AND DIOMED 30PLUS LASERS
DIOMED, INC.                      510(k) NO: K013499(SPECIAL)
ATTN: MARY  MCNAMARA-CULLINANE    PHONE NO : 508-643-0434
49 PLAIN STREET                   SE DECISION MADE: 16-NOV-01
NORTH ATTLEBORO, MA 02760         510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: DISETRONIC PENFINE INSULIN INJECTION PEN NEEDLE
DISETRONIC MEDICAL SYSTEMS        510(k) NO: K013782(TRADITIONAL)
ATTN: DAVID E CHADWICK            PHONE NO : 763-795-5200
5151 PROGRAM AVENUE               SE DECISION MADE: 20-NOV-01
ST. PAUL, MN 55112-1014           510(k) SUMMARY AVAILABLE FROM FDA

 
DEVICE: DORNIER SAPPHIREERBIUM HANDPIECE, DORNIER SAPPHIRESPOT HANDPIECE
DORNIER MEDICAL SYSTEMS, INC.     510(k) NO: K011322(TRADITIONAL)
ATTN: BRIAN  WALSH                PHONE NO : 770-514-6204
1155 ROBERTS BLVD.                SE DECISION MADE: 19-NOV-01
KENNESAW, GA 30144                510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: DYNAREX UMBILICAL CORD LAMP, MODELS 6833 AND 6833-B
DYNAREX CORP.                     510(k) NO: K012917(TRADITIONAL)
ATTN: JOHN  GAGLIARDI             PHONE NO : 513-573-0085
7736 WOODSIDE COURT               SE DECISION MADE: 28-NOV-01
MAINEVILLE, OH 45039              510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: EBI SPINELINK - II SPINAL FIXATION SYSTEM
EBI, L.P.                         510(k) NO: K012516(TRADITIONAL)
ATTN: PATRICIA M FLOOD            PHONE NO : 973-299-9300
100 INTERPACE PKWY.               SE DECISION MADE: 27-NOV-01
PARSIPPANY, NJ 07054-1079         510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: EBI XFIX DFS SYSTEM
EBI, L.P.                         510(k) NO: K013378(SPECIAL)
ATTN: MICHAEL T TAGGART           PHONE NO : 973-299-9300
100 INTERPACE PKWY.               SE DECISION MADE: 08-NOV-01
PARSIPPANY, NJ 07054-1079         510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: EBI XFIX ACCESS PELVIC FIXATOR
EBI, L.P.                         510(k) NO: K013540(SPECIAL)
ATTN: MICHAEL  TAGGART            PHONE NO : 973-299-9022
100 INTERPACE PKWY.               SE DECISION MADE: 20-NOV-01
PARSIPPANY, NJ 07054-1079         510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: EFILM VIDEO
EFILM MEDICAL, INC.               510(k) NO: K013631(TRADITIONAL)
ATTN: JOSEPH A THOMAS             PHONE NO : 416 204 9664
500 UNIVERSITY AVE., SUITE 300    SE DECISION MADE: 20-NOV-01
TORONTO, ONTARIO, CANADA M5G 1V7  510(k) SUMMARY AVAILABLE FROM FDA
                                  THIRD PARTY REVIEW

DEVICE: ATAC PAK DIRECT HDL REAGENT AND ATAC DIRECT HDL CALIBRATOR KITS
ELAN HOLDINGS, INC.               510(k) NO: K013152(TRADITIONAL)
ATTN: WYNN  STOCKING              PHONE NO : 714-672-3553
1075 W. LAMBERT RD., SUITE D      SE DECISION MADE: 09-NOV-01
BREA, CA 92821                    510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: SURGITRON 120 IEC (ALSO KNOWN AS SURGITRON 4.0 DUAL RF
ELLMAN INTL., INC.                510(k) NO: K013255(TRADITIONAL)
ATTN: FRANK  LIN                  PHONE NO : 516-569-1482
1135 RAILROAD AVE.,               SE DECISION MADE: 07-NOV-01
ELLMAN BLDG.                      510(k) SUMMARY AVAILABLE FROM FDA
HEWLETT, NY 11557

DEVICE: PASS SPINAL SYSTEM
ENCORE ORTHOPEDICS, INC.          510(k) NO: K013431(SPECIAL)
ATTN: JOANNA  DROEGE              PHONE NO : 512-832-9500
9800 METRIC BLVD.                 SE DECISION MADE: 15-NOV-01
AUSTIN, TX 78758                  510(k) SUMMARY AVAILABLE FROM FDA

 
DEVICE: TRI-FIX SPINAL FIXATION SYSTEM
ENDIUS, INC.                      510(k) NO: K013403(SPECIAL)
ATTN: SUSAN  FINNERAN             PHONE NO : 508-643-0983
23 WEST BACON ST.                 SE DECISION MADE: 14-NOV-01
PLAINVILLE, MA 02762              510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: TISSUE GRASPING FORCEPS, SCISSORS, CLAMPS AND DISSECTORS FOR LAP
ENDO-THERAPEUTICS, INC.           510(k) NO: K012725(TRADITIONAL)
ATTN: TODD  ADKISSON              PHONE NO : 727-726-2446
1183 CEDAR ST.                    SE DECISION MADE: 08-NOV-01
SAFETY HARBOR, FL 34695-2908      510(k) STATEMENT

DEVICE: VARICES INJECTION NEEDLE
ENDO-THERAPEUTICS, INC.           510(k) NO: K012977(TRADITIONAL)
ATTN: TODD  ADKISSON              PHONE NO : 727-726-2446
1183 CEDAR ST.                    SE DECISION MADE: 02-NOV-01
SAFETY HARBOR, FL 34695-2908      510(k) STATEMENT

DEVICE: OXYGEN APPLIED SYMPTOM IMPROVEMENT SYSTEM (OASIS)
ENGINEERED MEDICAL TECHNOLOGY, INC510(k) NO: K001121(ABBREVIATED)
ATTN: DON  SCHMIELEY              PHONE NO : 361-578-3551
7303 HOUSTON HWY.                 SE DECISION MADE: 29-NOV-01
P.O. BOX 1939                     510(k) SUMMARY AVAILABLE FROM FDA
VICTORIA, TX 77902

DEVICE: MOLDED CRANIAL HELMET
FAIRVIEW ORTHOPEDIC LABORATORY    510(k) NO: K012920(TRADITIONAL)
ATTN: ROSS C D'EMANUELE           PHONE NO : 612-343-2161
220 S.6TH STREET                  SE DECISION MADE: 28-NOV-01
MINNEAPOLIS, MN 55402-1498        510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: PARADIGM-FONTONA PEROVSKITE ND: YAP LASER SYSTEM AND ACCESSORIES
FOTONA D.D.                       510(k) NO: K011174(TRADITIONAL)
ATTN: MOJCA  VALJAVEC             PHONE NO : 386 151 11215
STEGNE 7,                         SE DECISION MADE: 07-NOV-01
1210 LJUBLJANA, SLOVENIA 1210     510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: DIACLEAR ULTRAFILTER
GAMBRO RENAL PRODUCTS             510(k) NO: K003957(TRADITIONAL)
ATTN: SUZANNE  DENNIS             PHONE NO : 303-542-5075
10810 W. COLLINS AVE.             SE DECISION MADE: 01-NOV-01
LAKEWOOD, CO 80215                510(k) STATEMENT

DEVICE: SIGNA OPENSPEED MAGNETIC RESONANCE SYSTEM
GE MEDICAL SYSTEM                 510(k) NO: K012875(TRADITIONAL)
ATTN: LARRY  KROGER               PHONE NO : 262-544-3894
3200 N. GRANDVIEW BLVD.           SE DECISION MADE: 20-NOV-01
WAUKESHA, WI 53188                510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: LIGHTSPEED 4.0 CT SCANNER SYSTEM
GE MEDICAL SYSTEM                 510(k) NO: K013561(TRADITIONAL)
ATTN: LARRY A KROGER              PHONE NO : 262-544-3894
16800 RYERSON ROAD                SE DECISION MADE: 08-NOV-01
NEW BERLIN, WI 53151              510(k) SUMMARY AVAILABLE FROM FDA
                                  THIRD PARTY REVIEW

 
DEVICE: DUAL ENERGY AND TISSUE EQUALIZATION SOFTWARE OPTION
GE MEDICAL SYSTEMS                510(k) NO: K013481(TRADITIONAL)
ATTN: JODI  PARKER                PHONE NO : 262-548-4964
3000 NORTH GRANDVIEW BLVD.        SE DECISION MADE: 02-NOV-01
WAUKESHA, WI 53188                510(k) SUMMARY AVAILABLE FROM FDA
                                  THIRD PARTY REVIEW

DEVICE: MODIFICATION TO COROMETRICS MODEL 120IS MATERNAL/FETAL MONITORIN
GE MEDICAL SYSTEMS INFORMATION TEC510(k) NO: K012718(TRADITIONAL)
ATTN: JOELLE  NEIDER              PHONE NO : 203-949-8232
61 BARNES PARK RD., NORTH         SE DECISION MADE: 13-NOV-01
WALLINGFORD, CT 06492             510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: GIMMI ALPHA SINUSCOPES MODEL # E.8282.01/31/71 + E.8284.01/31/71
GIMMI GMBH                        510(k) NO: K013731(TRADITIONAL)
ATTN: DAGMAR S MASER              PHONE NO : 312 042 89591
AMSTEL 320-I                      SE DECISION MADE: 27-NOV-01
AMSTERDAM, NETHERLANDS 1017AP     510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: ANEURYSM CLIPS
GISTLSTRASSE                      510(k) NO: K013136(TRADITIONAL)
ATTN: DIETER VON  SEPPELIN        PHONE NO : 498 979 36880
GISTLSTRASSE 99                   SE DECISION MADE: 26-NOV-01
PULLACH, GERMANY 82049            510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: FAS SET #4551
GYNETICS MEDICAL PRODUCTS NV      510(k) NO: K013497(TRADITIONAL)
ATTN: GRACE  HOLLAND              PHONE NO : 949-262-0411
3722 AVE. SAUSALITO               SE DECISION MADE: 09-NOV-01
IRVINE, CA 92606                  510(k) STATEMENT

DEVICE: IUI, MODEL 4220; SMOOZE, MODEL 4225, L; SEMINOR, MODEL 4502 A, B
GYNETICS MEDICAL PRODUCTS NV      510(k) NO: K013501(TRADITIONAL)
ATTN: GRACE  HOLLAND              PHONE NO : 949-262-0411
3722 AVE. SAUSALITO               SE DECISION MADE: 30-NOV-01
IRVINE, CA 92606                  510(k) STATEMENT

DEVICE: EMTRAC; DELPHIN; SEMTRAC 2000 SET
GYNETICS MEDICAL PRODUCTS NV      510(k) NO: K013536(TRADITIONAL)
ATTN: GRACE  HOLLAND              PHONE NO : 949-262-0411
3722 AVE. SAUSALITO               SE DECISION MADE: 30-NOV-01
IRVINE, CA 92606                  510(k) STATEMENT

DEVICE: TWINTRODE ELC 134 ELECTRODE
HEALTH TRONICS SURGICAL SERVICES, 510(k) NO: K012785(TRADITIONAL)
ATTN: PETER  WEIMAN               PHONE NO : 770-419-0691
1841 WEST OAK PARKWAY, SUITE A    SE DECISION MADE: 16-NOV-01
MARIETTA, GA 30062                510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: CLIP PARTIAL PROSTHESIS-TITANIUM DRESDEN, MODEL 1002 250-257
HEINZ KURZ GMBH MEDIZINTECHNIK    510(k) NO: K013573(SPECIAL)
ATTN: DAGMAR S MASER              PHONE NO : 312 042 89591
AMSTEL 320-I                      SE DECISION MADE: 09-NOV-01
AMSTERDAM, NETHERLANDS 1017 AP    510(k) SUMMARY AVAILABLE FROM FDA

 
DEVICE: HILL-ROM PRIMAVIEW MONITOR SYSTEM
HILL-ROM, INC.                    510(k) NO: K013709(TRADITIONAL)
ATTN: TIMOTHY M DAVIS             PHONE NO : 800-445-2114
1069 STATE RT. 46 EAST            SE DECISION MADE: 16-NOV-01
BATESVILLE, IN 47006              510(k) SUMMARY AVAILABLE FROM FDA
                                  THIRD PARTY REVIEW

DEVICE: ICONNECTION 3D
HINNOVATION, INC.                 510(k) NO: K012779(TRADITIONAL)
ATTN: YI ISABELLE  SUN            PHONE NO : 414-453-7881
10437 INNOVATION DRIVE            SE DECISION MADE: 02-NOV-01
SUITE 236                         510(k) SUMMARY AVAILABLE FROM FDA
WAUWATOSA, WI 53226-4815

DEVICE: DURACON CONSTRAINED POSTERIOR STABILIZED (PS) TIBIAL INSERT
HOWMEDICA OSTEONICS CORP.         510(k) NO: K012776(TRADITIONAL)
ATTN: MARGARET F CROWE            PHONE NO : 201-934-4359
59 ROUTE 17                       SE DECISION MADE: 16-NOV-01
ALLENDALE, NJ 07401               510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: LONG LENGTH DYAX NAIL
HOWMEDICA OSTEONICS CORP.         510(k) NO: K013468(SPECIAL)
ATTN: KAREN  ARIEMMA              PHONE NO : 201-760-8187
59 ROUTE 17                       SE DECISION MADE: 16-NOV-01
ALLENDALE, NJ 07401-1677          510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: TROCHANTERIC DYAX NAIL SYSTEM
HOWMEDICA OSTEONICS CORP.         510(k) NO: K013524(SPECIAL)
ATTN: KAREN  ARIEMMA              PHONE NO : 201-760-8187
59 ROUTE 17                       SE DECISION MADE: 14-NOV-01
ALLENDALE, NJ 07401-1677          510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: RELISA PR3-ANCA TEST SYSTEM FOR ANTIBODIES TO PROTEINASE 3, MODE
IMMUNO CONCEPTS, INC.             510(k) NO: K013283(TRADITIONAL)
ATTN: ERIC S HOY                  PHONE NO : 972-247-3616
2280 SPRINGLAKE ROAD              SE DECISION MADE: 14-NOV-01
SUITE 106                         510(k) SUMMARY AVAILABLE FROM FDA
DALLAS, TX 75234

DEVICE: RELISA MPO-ANCA TEST SYSTEM FOR ANTIBODIES TO MYELOPEROXIDASE, M
IMMUNO CONCEPTS, INC.             510(k) NO: K013285(TRADITIONAL)
ATTN: ERIC S  HOY                 PHONE NO : 972-247-3616
2280 SPRINGLAKE ROAD              SE DECISION MADE: 14-NOV-01
SUITE 106                         510(k) SUMMARY AVAILABLE FROM FDA
DALLAS, TX 75234

DEVICE: IGG ANTI-NDNA FLUORESCENT TEST SYSTEM; MODEL # 3040G
IMMUNO CONCEPTS, INC.             510(k) NO: K013432(TRADITIONAL)
ATTN: ERIC S HOY                  PHONE NO : 916-363-2649
9779 BUSINESS PARK DR.            SE DECISION MADE: 29-NOV-01
SUITE D                           510(k) SUMMARY AVAILABLE FROM FDA
SACRAMENTO, CA 95827

 
DEVICE: QWIKSIM VIRTUAL SIMULATION SYSTEM; VERSION 2.00
IMPAC MEDICAL SYSTEMS, INC.       510(k) NO: K013531(TRADITIONAL)
ATTN: THOMAS H FARIS              PHONE NO : 650-623-8807
100 WEST EVELYN AVE.              SE DECISION MADE: 07-NOV-01
MOUNTAIN VIEW, CA 94041           510(k) SUMMARY AVAILABLE FROM FDA
                                  THIRD PARTY REVIEW

DEVICE: ULTRA THICK MALE LATEX CONDOM WITH SILICONE LUBRICANT
INNOLATEX SDN. BHD                510(k) NO: K012664(TRADITIONAL)
ATTN: CHANG  AH-KAU               PHONE NO : 603 747 2434
NO 16, JALAN BULAN U5/5           SE DECISION MADE: 09-NOV-01
BANDAR PINGGIRAN SUBANG,          510(k) STATEMENT
SHAH ALAM,SELANGOR DARUL EHSAN, MALAYSIA

DEVICE: ULTRA THIN MALE LATEX CONDOM WITH SILICONE LUBRICANT
INNOLATEX SDN. BHD                510(k) NO: K012665(TRADITIONAL)
ATTN: CHANG  AH-KAU               PHONE NO : 603 747 2434
NO 16, JALAN BULAN U5/5           SE DECISION MADE: 09-NOV-01
BANDAR PINGGIRAN SUBANG,          510(k) STATEMENT
SHAH ALAM,SELANGOR DARUL EHSAN, MALAYSIA

DEVICE: DOTTED CONDOM, MALE NATURAL RUBBER LATEX CONDOM
INNOLATEX SDN. BHD                510(k) NO: K012962(ABBREVIATED)
ATTN: CHANG  AH-KAU               PHONE NO : 603 747 2434
NO 16, JALAN BULAN U5/5           SE DECISION MADE: 09-NOV-01
BANDAR PINGGIRAN SUBANG,          510(k) STATEMENT
SHAH ALAM,SELANGOR DARUL EHSAN, MALAYSIA

DEVICE: 56MM CONDOM,MALE NATURAL RUBBER LATEX CONDOM
INNOLATEX SDN. BHD                510(k) NO: K012964(ABBREVIATED)
ATTN: CHANG  AH-KAU               PHONE NO : 603 747 2434
NO. 16, JALAN BULAN U5/5,         SE DECISION MADE: 09-NOV-01
BANDAR PINGGIRAN SUBANG           510(k) STATEMENT
SHAH ALAM, SELANGOR D.E., MALAYSIA 40150

DEVICE: IQUANTIFY, VERSION 1.0
INSIGTHFUL CORP.                  510(k) NO: K011196(TRADITIONAL)
ATTN: BRADLEY T WYMAN             PHONE NO : 206-283-8802
1700 WESTLAKE AVE.                SE DECISION MADE: 08-NOV-01
SUITE 500                         510(k) SUMMARY AVAILABLE FROM FDA
SEATTLE, WA 98109-3044

DEVICE: TELESCOPIC PLATE SPACER THORACOLUMBAR (TPS-TL) SPINAL, MODEL 811
INTERPORE CROSS INTL.             510(k) NO: K010989(TRADITIONAL)
ATTN: LYNN R RODARTI              PHONE NO : 949-453-3200
181 TECHNOLOGY DR.                SE DECISION MADE: 07-NOV-01
IRVINE, CA 92618-2402             510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: INTUITIVE SURGICAL BIPOLAR FORCEPS
INTUITIVE SURGICAL, INC.          510(k) NO: K012833(TRADITIONAL)
ATTN: MICHAEL  YRAMATEGUI         PHONE NO : 659-237-7000
1340 WEST MIDDLEFIELD RD.         SE DECISION MADE: 16-NOV-01
MOUNTAIN VIEW, CA 94043           510(k) SUMMARY AVAILABLE FROM FDA

 
DEVICE: ONE TOUCH FASTTAKE COMPACT BLOOD GLUCOSE MONITORING SYSTEM, ONE
INVERNESS MEDICAL TECHNOLOGY, INC.510(k) NO: K011479(TRADITIONAL)
ATTN: CAROL A ADILETTO            PHONE NO : 781-647-3900
51 SAWYER ROAD                    SE DECISION MADE: 30-NOV-01
SUITE 200                         510(k) SUMMARY AVAILABLE FROM FDA
WALTHAM, MA 02453-3448

DEVICE: WATCH-PAT 100
ITAMAR MEDICAL (C.M.) 1997 LTD.   510(k) NO: K010739(TRADITIONAL)
ATTN: GEORGE  MYERS               PHONE NO : 201-727-1703
377 ROUTE 17                      SE DECISION MADE: 06-NOV-01
HASBROUCK HEIGHTS, NJ 07604       510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: HIGH GOLD PALLADIUM FREE CERAMIC SOLDER
IVOCLAR USA, INC.                 510(k) NO: K012877(TRADITIONAL)
ATTN: ANDERJEET  GULATI           PHONE NO : 800-533-6825
175 PINEVIEW DR.                  SE DECISION MADE: 21-NOV-01
AMHERST, NY 14150                 510(k) STATEMENT

DEVICE: JOSTRA ARTERIAL PERFUSION CANNULAE, MODEL A...
JOSTRA AG                         510(k) NO: K012617(TRADITIONAL)
ATTN: KATHLEEN  JOHNSON           PHONE NO : 610-932-7738
P.O. BOX 218                      SE DECISION MADE: 06-NOV-01
OXFORD, PA 19363                  510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: JOSTRA ARTERIAL PERFUSION CANNULAE
JOSTRA AG                         510(k) NO: K012774(TRADITIONAL)
ATTN: KATHLEEN  JOHNSON           PHONE NO : 610-932-7738
478 MEDIA ROAD                    SE DECISION MADE: 16-NOV-01
OXFORD, PA 19363                  510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: KADANCE 2000
KADA RESEARCH, INC.               510(k) NO: K012492(TRADITIONAL)
ATTN: HARVEY  KNAUSS              PHONE NO : 713-723-4080
11874 SOUTH EVELYN CIRCLE         SE DECISION MADE: 02-NOV-01
HOUSTON, TX 77071-3404            510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: KSEA SIALOENDOSCOPES AND ACCESSORIES
KARL STORZ ENDOSCOPY-AMERICA, INC.510(k) NO: K012527(TRADITIONAL)
ATTN: JAMES A LEE                 PHONE NO : 310-410-2769
600 CORPORATE POINTE              SE DECISION MADE: 01-NOV-01
CULVER CITY, CA 90230-7600        510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: SAFESKIN HEALTHTOUCH POWDER-FREE EXAM GLOVE WITH VITAMIN E AND A
KIMBERLY-CLARK CORP.              510(k) NO: K012815(TRADITIONAL)
ATTN: MARCIA  JOHNSON             PHONE NO : 770-587-8324
1400 HOLCOMB BRIDGE RD.           SE DECISION MADE: 13-NOV-01
ROSWELL, GA 30076                 510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: STARS2000 POWER CANNULA
KMI KOLSTER METHODS, INC.         510(k) NO: K012236(TRADITIONAL)
ATTN: ALWIN H KOLSTER             PHONE NO : 714-956-1964
1170 N. GILBERT ST.               SE DECISION MADE: 19-NOV-01
ANAHEIM, CA 92801                 510(k) STATEMENT

 
DEVICE: LERMAN & SON CRANIAL ORTHOSIS HELMET
LERMAN & SON                      510(k) NO: K012830(TRADITIONAL)
ATTN: MAX  LERMAN                 PHONE NO : 310-659-2290
8710 WILSHIRE BLVD.               SE DECISION MADE: 20-NOV-01
BEVERLY HILLS, CA 90211           510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: RESECTION ABLATOR
LINVATEC CORP.                    510(k) NO: K013117(TRADITIONAL)
ATTN: LAURA D SENEFF              PHONE NO : 727-399-5234
11311 CONCEPT BOULEVARD           SE DECISION MADE: 29-NOV-01
LARGO, FL 34643                   510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: ARAMIS DERMATLOGIC LASER
LUMEDICS, LTD.                    510(k) NO: K012545(TRADITIONAL)
ATTN: JONATHAN S KAHAN            PHONE NO : 202-637-5794
555 THIRTEEN STREET N.W.          SE DECISION MADE: 05-NOV-01
WASHINGTON, DC 20004              510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: VALIDATE CHEM 6 CALIBRATION VERIFICATION TEST SET MODEL # 10006
MAINE STANDARDS CO.               510(k) NO: K013119(TRADITIONAL)
ATTN: CHRISTINE  BEACH            PHONE NO : 207-892-1300
765 ROOSEVELT TRAIL               SE DECISION MADE: 16-NOV-01
WINDHAM, ME 04062-5365            510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: VALIDATE CHEM 7 CALIBRATION VERIFICATION TEST SET, MODEL 10007
MAINE STANDARDS CO.               510(k) NO: K013265(TRADITIONAL)
ATTN: CHRISTINE  BEACH            PHONE NO : 207-892-1300
765 ROOSEVELT TRAIL               SE DECISION MADE: 20-NOV-01
WINDHAM, ME 04062-5365            510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: MAROSIS PACS
MAROTECH, INC                     510(k) NO: K012844(TRADITIONAL)
ATTN: CARL  ALLETTO               PHONE NO : 940-440-9530
2001 EAST OAKSHORES DRIVE         SE DECISION MADE: 08-NOV-01
CROSSROADS, TX 76227              510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: POWDERED LATEX MEDICAL MEDICAL EXAMINATION GLOVES WITH 150 MICRO
MAXTER GLOVE MANUFACTURING SDN BHD 510(k) NO: K013443(TRADITIONAL)
ATTN: STANLEY  THAI               PHONE NO : 001 301 4438913
LOT 607, JALAN HAJI ABDUL         SE DECISION MADE: 29-NOV-01
MANAN                             510(k) SUMMARY AVAILABLE FROM FDA
41050 KLANG, SELANGOR, MALAYSIA 41050

DEVICE: COMFORTCARE COMPRESSION SUPPORT WITH MAGNETS COMFORTCARE MAGNETI
MED GEN, INC.                     510(k) NO: K013239(TRADITIONAL)
ATTN: THEODORE  BARASH            PHONE NO : 561-740-1100
7284 W. PALMETTO PK. RD.          SE DECISION MADE: 20-NOV-01
BOCA RATON, FL 33433-3406         510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: REPROCESSED ARTHROSCOPIC BLADES, ARTHROSCOPIC SHAVERS, SHAVER BL
MEDICAL INSTRUMENTS TECHNOLOGY, IN510(k) NO: K012624(TRADITIONAL)
ATTN: JACK  SPEER                 PHONE NO : 435-674-4010
385 NORTH 3050 EAST, SUITE B      SE DECISION MADE: 08-NOV-01
ST. GEORGE, UT 84790              510(k) SUMMARY AVAILABLE FROM FDA


DEVICE: SONOACE SA-8000 DIAGNOSTIC ULTRASOUND SYSTEM
MEDISON AMERICA, INC.             510(k) NO: K013627(TRADITIONAL)
ATTN: A. ROBERT  DEPALMA          PHONE NO : 714-889-3000
11075 KNOTT AVE.                  SE DECISION MADE: 16-NOV-01
CYPRESS, CA 90630-5135            510(k) SUMMARY AVAILABLE FROM FDA
                                  THIRD PARTY REVIEW

DEVICE: POWER DRIVE
MEDITEAM AB                       510(k) NO: K012944(TRADITIONAL)
ATTN: THOMAS  STJERNKVIST         PHONE NO : 46 31 3369103
GOTEBORGSVAGEN 74,                SE DECISION MADE: 20-NOV-01
SAVEDALEN, SWEDEN S-433 63        510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: MEDSTAR 150
MEDNET SERVICES, INC.             510(k) NO: K013081(TRADITIONAL)
ATTN: DAVID L MATHEWS             PHONE NO : 612-788-6228
2855 ANTHONY LN. SOUTH, #B10      SE DECISION MADE: 20-NOV-01
ST. ANTHONY, MN 55418             510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: MEDSTAR 100 INTERFERENTIAL STIMLATOR
MEDNET SERVICES, INC.             510(k) NO: K013082(TRADITIONAL)
ATTN: DAVID L  MATHEWS            PHONE NO : 612-788-6228
2855 ANTHONY LN. SOUTH, #B10      SE DECISION MADE: 16-NOV-01
ST. ANTHONY, MN 55418             510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: STENT SUPPORT GUIDE CATHETER
MEDTRONIC, INC.                   510(k) NO: K010579(TRADITIONAL)
ATTN: FRED L BOUCHER              PHONE NO : 978-777-0042
37A CHERRY HILL DRIVE             SE DECISION MADE: 21-NOV-01
DANVERS, MA 01923                 510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: GIOTTO IMAGE
MEDX, INC.                        510(k) NO: K012953(TRADITIONAL)
ATTN: FLOYD R ROWAN               PHONE NO : 847-463-2020
3456 N. RIDGE AVE., #100          SE DECISION MADE: 30-NOV-01
ARLINGTON HEIGHTS, IL 60004       510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: LYMPHA PRESS PLUS DEVICE
MEGO AFEK                         510(k) NO: K013331(TRADITIONAL)
ATTN: AHAVA  STEIN                PHONE NO : 972 976 70002
BEIT HAPA'AMON (BOX 124)          SE DECISION MADE: 30-NOV-01
20 HATA'AS ST.                    510(k) SUMMARY AVAILABLE FROM FDA
KFAR SABA, ISRAEL 44425

DEVICE: MICRO STAMPING LIGATING CLIP
MICRO STAMPING CORP.              510(k) NO: K013264(TRADITIONAL)
ATTN: JOHN  GAGLIARDI             PHONE NO : 513-573-0085
7736 WOODSIDE COURT               SE DECISION MADE: 29-NOV-01
MAINEVILLE, OH 45039              510(k) SUMMARY AVAILABLE FROM FDA

 
DEVICE: PERIOLASE ND:YAG DENTAL LASER SYSTEM
MILLENNIUM DENTAL TECHNOLOGIES, IN510(k) NO: K010771(TRADITIONAL)
ATTN: DAVID M HARRIS              PHONE NO : 510-583-7574
4256 HEYER AVENUE                 SE DECISION MADE: 27-NOV-01
CASTRO VALLEY, CA 94546           510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: DISPOSABLE STORAGE CAP
MOLDED PRODUCTS                   510(k) NO: K010366(ABBREVIATED)
ATTN: ELISE  JOHNSTON             PHONE NO :
P.O. BOX 15                       SE DECISION MADE: 28-NOV-01
HARLAN, IA 51537                  510(k) STATEMENT

DEVICE: DRT4 LASER DOPPLER PERFUSION AND TEMPERATURE MONITOR
MOOR INSTRUMENTS LTD.             510(k) NO: K011070(TRADITIONAL)
ATTN: DAVID  BOGGETT              PHONE NO : 440 129 735715
MILLWEY                           SE DECISION MADE: 07-NOV-01
AXMINSTER, DEVON, UNITED KINGDOM E510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: HRH-127-ALLEGRA HEAD ARRAY COIL
MRI DEVICES CORP.                 510(k) NO: K013508(SPECIAL)
ATTN: THOMAS  SCHUBERT            PHONE NO : 262-524-1402
1515 PARAMOUNT DR. SUITE A        SE DECISION MADE: 20-NOV-01
WAUKESHA, WI 53186                510(k) STATEMENT

DEVICE: HNC-63-INT NEUROVASCULAR ARRAY COIL
MRI DEVICES CORP.                 510(k) NO: K013602(SPECIAL)
ATTN: THOMAS  SCHUBERT            PHONE NO : 262-524-1402
1515 PARAMOUNT DR. SUITE A        SE DECISION MADE: 20-NOV-01
WAUKESHA, WI 53186                510(k) STATEMENT

DEVICE: MODEL NT-360 RANGE OF MOTION
MYOTRONICS-NOROMED, INC.          510(k) NO: K013357(SPECIAL)
ATTN: FRAY  ADIB                  PHONE NO : 800-426-0316
15425 53RD AVE. SOUTH             SE DECISION MADE: 08-NOV-01
TUKWILA, WA 98188                 510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: MODEL MES-9000/EMG SYSTEM
MYOTRONICS-NOROMED, INC.          510(k) NO: K013399(SPECIAL)
ATTN: FRAY  ADIB                  PHONE NO : 206-243-4214
15425 53RD AVE. SOUTH             SE DECISION MADE: 13-NOV-01
TUKWILA, WA 98188                 510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: N2000 BASE STATION, N2001 NURSE STATION
NEPTEC DESIGN GROUP, LTD.         510(k) NO: K012801(TRADITIONAL)
ATTN: CHARLES H KYPER             PHONE NO : 919-960-0049
103 NOLEN LANE                    SE DECISION MADE: 14-NOV-01
CHAPEL HILL, NC 27516             510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: MODIFICATION TO HANDMASTER
NESS-NEUROMUSCULAR ELECTRICAL STIM510(k) NO: K012823(TRADITIONAL)
ATTN: JONATHAN S HAHAN            PHONE NO : 202-637-5794
555 13TH STREET, N.W.             SE DECISION MADE: 14-NOV-01
WASHINGTON, DC 20004-1109         510(k) SUMMARY AVAILABLE FROM FDA

 
DEVICE: 3CC NMT SAFETY SYRINGE
NEW MEDICAL TECHNOLOGY LTD.       510(k) NO: K010819(TRADITIONAL)
ATTN: MIKE  MALANDRAKIS           PHONE NO : 317-773-9560
1500 WEST OAK STREET              SE DECISION MADE: 08-NOV-01
PO BOX 317                        510(k) SUMMARY AVAILABLE FROM FDA
ZIONSVILLE, IN 46077

DEVICE: INFUSION IV SET
NIRVI INTL. USA                   510(k) NO: K001879(TRADITIONAL)
ATTN: DARSHANA  HATHI             PHONE NO : 412-854-5531
467 DIABLO DR.                    SE DECISION MADE: 20-NOV-01
PITTSBURG, PA 15241               510(k) STATEMENT

DEVICE: NORDIX INC RECHARGEABLE BATTERY PART NUMBER 2116
NORDIX, INC.                      510(k) NO: K013133(TRADITIONAL)
ATTN: MARIAN  LISAK               PHONE NO : 602-544-1690
6831 NORTH 21ST AVE.              SE DECISION MADE: 13-NOV-01
PHOENIX, AZ 85015                 510(k) STATEMENT

DEVICE: TCM ENDO III
NOUVAG AG                         510(k) NO: K013185(TRADITIONAL)
ATTN: COLLEEN  BOSWELL            PHONE NO : 714-516-7484
1717 WEST COLLINS AVENUE          SE DECISION MADE: 28-NOV-01
ORANGE, CA 92867                  510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: BODY FAT ANALYZER, MODEL HBF-306
OMRON HEALTHCARE, INC.            510(k) NO: K011652(TRADITIONAL)
ATTN: OSAMU  SHIRASAKI            PHONE NO : 847-680-6200
300 LAKEVIEW PKWY.                SE DECISION MADE: 07-NOV-01
VERNON HILLS, IL 60061            510(k) STATEMENT

DEVICE: MICROSTREAM O2/CO2 ORAL NASAL FILTERLINE
ORIDION MEDICAL 1987 LTD.         510(k) NO: K011536(SPECIAL)
ATTN: SANFORD  BROWN              PHONE NO : 972 2 5899115
7 HAMARPE ST. P.O. BOX 45025      SE DECISION MADE: 14-NOV-01
HAR HOTZVIM INDUSTRIAL PARK       510(k) SUMMARY AVAILABLE FROM FDA
JERUSALEM, ISRAEL 91450

DEVICE: MODIFICATION TO: MAC-LINE O2/CO2 ORAL NASAL CANNULA SAMPLE LINE
ORIDION MEDICAL 1987 LTD.         510(k) NO: K013845(SPECIAL)
ATTN: SANFORD  BROWN              PHONE NO : 972 258 99115
7 HAMARPE ST. P.O. BOX 45025      SE DECISION MADE: 29-NOV-01
HAR HOTZVIM INDUSTRIAL PARK       510(k) SUMMARY AVAILABLE FROM FDA
JERUSALEM, ISRAEL 91450

DEVICE: HEALOS BONE GRAFT MATERIAL
ORQUEST, INC.                     510(k) NO: K012751(TRADITIONAL)
ATTN: KRISTINE F LAHMAN           PHONE NO : 650-237-4852
365 RAVENDALE DRIVE               SE DECISION MADE: 14-NOV-01
MOUNTAIN VIEW, CA 94043-5712      510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: OSI MEDICAL DOLPHIN STAND-ALONE PULSE OXIMETER & DIGITAL DOLPHIN
OSI MEDICAL, INC.                 510(k) NO: K012626(TRADITIONAL)
ATTN: JON  WERNER                 PHONE NO : 813-818-7488
13801 MCCORMICK DRIVE             SE DECISION MADE: 02-NOV-01
TAMPA, FL 33626                   510(k) SUMMARY AVAILABLE FROM FDA

 
DEVICE: OSMETECH MICROBIAL ANALYSER-URINARY TRACT INFECTION DETECTOR (OM
OSMETECH                          510(k) NO: K011043(TRADITIONAL)
ATTN: JOHN  PLANT                 PHONE NO : 441 270 216444
ELECTRA HOUSE ELECTRA WAY         SE DECISION MADE: 30-NOV-01
CREWE, UNITED KINGDOM CW1 6WZ     510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: AUTOJECT 2
OWEN MUMFORD USA, INC.            510(k) NO: K013362(TRADITIONAL)
ATTN: ROBERT  SHAW                PHONE NO : 770-425-5138
1755-A WEST OAK COMMONS CT.       SE DECISION MADE: 13-NOV-01
MARIETTA, GA 30062                510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: MULTISTIM
PAJUNK GMBH                       510(k) NO: K011308(TRADITIONAL)
ATTN: LYNETTE  HOWARD             PHONE NO : 908-788-4580
203 MAIN STREET, PMB 166          SE DECISION MADE: 29-NOV-01
FLEMINGTON,, NJ 08822             510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: TROCAR SLEEVE AND ACCESSORIES, MODELS 1287-XX-XX
PAJUNK GMBH                       510(k) NO: K012771(TRADITIONAL)
ATTN: MARTIN  HANGER              PHONE NO : 497 704 92910
AM HOLZPLATZ 5-7                  SE DECISION MADE: 14-NOV-01
GEISINGEN, GERMANY D-78187        510(k) SUMMARY AVAILABLE FROM FDA
                                  THIRD PARTY REVIEW

DEVICE: LIVESURE METHADONE SCREEN TESTS
PAN PROBE BIOTECH, INC.           510(k) NO: K013796(TRADITIONAL)
ATTN: ALICE H YU                  PHONE NO : 858-689-9936
8515 ARJONS DR., SUITE A          SE DECISION MADE: 26-NOV-01
SAN DIEGO, CA 92126               510(k) SUMMARY AVAILABLE FROM FDA
                                  THIRD PARTY REVIEW

DEVICE: TONOPORT V
PAR MEDIZINTECHNIK GMBH           510(k) NO: K012647(ABBREVIATED)
ATTN: LOTHAR  ENGEL               PHONE NO : 493 023 50700
EINEMSTRASSE 9                    SE DECISION MADE: 09-NOV-01
BERLIN, GERMANY D-10787           510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: KP + LFM
PDS HEALTHCARE PRODUCTS, INC.     510(k) NO: K013489(TRADITIONAL)
ATTN: JIM  LEWIS                  PHONE NO : 303-666-6340
908 MAIN ST.                      SE DECISION MADE: 29-NOV-01
LOUISVILLE, CO 80027              510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: PF 5050 PRESSURE UNIT, MODEL PF 5050
PERIMED AB                        510(k) NO: K011899(TRADITIONAL)
ATTN: BJORN  BAKKEN               PHONE NO : 011 468 58011990
DATAVAGEN 9-A                     SE DECISION MADE: 06-NOV-01
JARFALLA, SWEDEN S-175 26         510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: PHILIPS COMPONENT COMPACT MONITOR,MODEL M1275B, PHILIPS COMPENEN
PHILIPS MEDICAL SYSTEMS, INC.     510(k) NO: K013199(SPECIAL)
ATTN: DAVE  OSBORN                PHONE NO : 978-659-3178
3000 MINUTEMAN RD.                SE DECISION MADE: 28-NOV-01
ANDOVER, MA 01810-1099            510(k) SUMMARY AVAILABLE FROM FDA

 
DEVICE: MODIFICATION TO:PHILIPS M3000A/M3046A COMPACT PORTABLE PATIENT M
PHILIPS MEDICAL SYSTEMS, INC.     510(k) NO: K013427(SPECIAL)
ATTN: DAVE  OSBORN                PHONE NO : 978-659-3178
3000 MINUTEMAN RD.                SE DECISION MADE: 29-NOV-01
ANDOVER, MA 01810-1099            510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: MODIFICATION TO M2376A DEVICELINK SYSTEM
PHILIPS MEDICAL SYSTEMS, INC.     510(k) NO: K013470(SPECIAL)
ATTN: MIKE  HUDON                 PHONE NO : 978-659-3173
3000 MINUTEMAN RD.                SE DECISION MADE: 14-NOV-01
ANDOVER, MA 01810-1099            510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: PHOENIX ELECTROLYTE CALIBRATION SET FOR THE MEDICAL EASYLYTE CAL
PHOENIX DIAGNOSTICS, INC.         510(k) NO: K012987(TRADITIONAL)
ATTN: RAM  NUNNA                  PHONE NO : 508-655-8310
8 TECH CIRCLE                     SE DECISION MADE: 07-NOV-01
NATICK, MA 01760                  510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: ZIPPY, MODEL I88WA
PILLAR TECHNOLOGY, INC.           510(k) NO: K012846(TRADITIONAL)
ATTN: CHRIS  TINSLEY              PHONE NO : 620-325-2629
1101 ILLINOIS                     SE DECISION MADE: 20-NOV-01
P.O. BOX 187                      510(k) STATEMENT
NEODESHA, KS 66757

DEVICE: HD/HDT, PV/PVT (POLYMACON) SOFT CONTACT LENS FOR DAILY WEAR (CLE
POLY VUE TECHNOLGIES, INC.        510(k) NO: K013220(TRADITIONAL)
ATTN: MARTIN  DALSING             PHONE NO : 970-243-5490
623 GLACIER DR.                   SE DECISION MADE: 20-NOV-01
GRAND JUNCTION, CO 81503          510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: BIOSCANNER 2000
POLYMER TECHNOLOGY SYSTEMS, INC.  510(k) NO: K013068(TRADITIONAL)
ATTN: MARGO  ENRIGHT              PHONE NO : 317-870-5610
7736 ZIONSVILLE RD.               SE DECISION MADE: 20-NOV-01
INDIANAPOLIS, IN 46268            510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: BIOSCANNER BEYOND GLUCOSE ANALYZER AND TEST STRIPS
POLYMER TECHNOLOGY SYSTEMS, INC.  510(k) NO: K013203(TRADITIONAL)
ATTN: MARGO  ENRIGHT              PHONE NO : 317-870-5610
7736 ZIONSVILLE RD.               SE DECISION MADE: 16-NOV-01
INDIANAPOLIS, IN 46268            510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: BOSS 2000-3 VACUUM ERECTION DEVICE
POS-T-VAC, INC.                   510(k) NO: K012670(TRADITIONAL)
ATTN: DENNIS L BELL               PHONE NO : 800-279-7434
1701 NORTH 14TH AVE.              SE DECISION MADE: 09-NOV-01
P.O. BOX 1436                     510(k) STATEMENT
DODGE CITY, KS 67801

DEVICE: BOSS-2000-2 VACUUM ERECTION DEVICE
POS-T-VAC, INC.                   510(k) NO: K012672(TRADITIONAL)
ATTN: DENNIS L BELL               PHONE NO : 316-227-7434
1701 NORTH 14TH AVE.              SE DECISION MADE: 09-NOV-01
P.O. BOX 1436                     510(k) STATEMENT
DODGE CITY, KS 67801

 
DEVICE: PRIME-DENT VISIBLE LIGHT CURE PIT & FISSURE SEALANT
PRIME DENTAL MANUFACTURING, INC.  510(k) NO: K012761(TRADITIONAL)
ATTN: ROLANDO  MARASIGAN          PHONE NO : 773-539-5927
3735 WEST BELMONT AVE.            SE DECISION MADE: 01-NOV-01
CHICAGO, IL 60618                 510(k) STATEMENT

DEVICE: PRIME-DENT CHEMICAL CURE PIT & FISSURE SEALANT
PRIME DENTAL MANUFACTURING, INC.  510(k) NO: K012794(TRADITIONAL)
ATTN: ROLANDO  MARASIGAN          PHONE NO : 773-539-5927
3735 WEST BELMONT AVE.            SE DECISION MADE: 05-NOV-01
CHICAGO, IL 60618                 510(k) STATEMENT

DEVICE: GLYCOSAL II HBA 1C TEST
PROVALIS DIAGNOSTICS LTD.         510(k) NO: K011933(TRADITIONAL)
ATTN: THOMAS M TSAKERIS           PHONE NO : 301-330-2076
16809 BRIARDALE ROAD              SE DECISION MADE: 02-NOV-01
ROCKVILLE, MD 20855               510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: PSYCHEMEDICS RIA COCAINE ASSAY
PSYCHEMEDICS CORP.                510(k) NO: K010868(TRADITIONAL)
ATTN: THOMAS  CAIRNS              PHONE NO : 310-216-7776
5832 UPLANDER WAY                 SE DECISION MADE: 06-NOV-01
CULVER CITY, CA 90230             510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: DYNAPULSE 500G (DP500G) BLLOD PRESSURE MONITORING SYSTEM
PULSE METRIC, INC.                510(k) NO: K012498(TRADITIONAL)
ATTN: ROBERT  DUFFY               PHONE NO : 858-480-1171
11777 SORRENTO VALLEY ROAD        SE DECISION MADE: 01-NOV-01
SAN DIEGO, CA 92121               510(k) STATEMENT

DEVICE: RECORDING AND STIMULATING ELECTRODE
RADIONICS, A DIVISION OF TYCO HEAL510(k) NO: K012850(TRADITIONAL)
ATTN: KEVIN J O'CONNELL           PHONE NO : 781-272-1233
22 TERRY AVE.                     SE DECISION MADE: 19-NOV-01
BURLINGTON, MA 01803              510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: BACTI-SWAB DRY
REMEL CO.                         510(k) NO: K013711(TRADITIONAL)
ATTN: ROBERT E BOOTH              PHONE NO : 913-888-0939
12076 SANTA FE DR.                SE DECISION MADE: 26-NOV-01
LENEXA, KS 66215                  510(k) STATEMENT

DEVICE: INFLUENZA A/B RAPID TEST, CAT NO 2158 663
ROCHE DIAGNOSTICS CORP.           510(k) NO: K011684(TRADITIONAL)
ATTN: LUANN  OCHS                 PHONE NO : 800-428-5074
9115 HAGUE RD.                    SE DECISION MADE: 30-NOV-01
P.O. BOX 50457                    510(k) SUMMARY AVAILABLE FROM FDA
INDIANAPOLIS, IN 46250-0457

DEVICE: TINA-QUANT COMPLEMENT C4 TEST SYSTEM
ROCHE DIAGNOSTICS CORP.           510(k) NO: K012359(TRADITIONAL)
ATTN: HELEN T TORNEY              PHONE NO : 800-428-5074
9115 HAGUE ROAD                   SE DECISION MADE: 29-NOV-01
INDIANAPOLIS, IN 46250-0457       510(k) SUMMARY AVAILABLE FROM FDA

 
DEVICE: TINA-QUANT COMPLEMENT C3C TEST SYSTEM
ROCHE DIAGNOSTICS CORP.           510(k) NO: K012361(TRADITIONAL)
ATTN: HELEN T TORNEY              PHONE NO : 800-428-5074
9115 HAGUE ROAD                   SE DECISION MADE: 29-NOV-01
INDIANAPOLIS, IN 46250-0457       510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: ONTRAK TESTCARD 9
ROCHE DIAGNOSTICS CORP.           510(k) NO: K012396(ABBREVIATED)
ATTN: JENNIFER  TRIBBETT          PHONE NO : 317-845-2000
9115 HAGUE ROAD                   SE DECISION MADE: 05-NOV-01
INDIANAPOLIS, IN 46256            510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: TINA-QUANT APOLIPOPROTEIN B VER.2
ROCHE DIAGNOSTICS CORP.           510(k) NO: K013206(TRADITIONAL)
ATTN: KAY A TAYLOR                PHONE NO : 317-521-3544
9115 HAGUE ROAD                   SE DECISION MADE: 16-NOV-01
INDIANAPOLIS, IN 46256            510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: TINA-QUANT APOLIPOPROTEIN B VER.2
ROCHE DIAGNOSTICS CORP.           510(k) NO: K013207(TRADITIONAL)
ATTN: KAY A TAYLOR                PHONE NO : 317-521-3544
9115 HAGUE ROAD                   SE DECISION MADE: 13-NOV-01
INDIANAPOLIS, IN 46256            510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: TINA-QUANT APOLIPOPROTEIN VER.2
ROCHE DIAGNOSTICS CORP.           510(k) NO: K013249(TRADITIONAL)
ATTN: HELEN T TORNEY              PHONE NO : 317-521-7634
9115 HAGUE ROAD                   SE DECISION MADE: 16-NOV-01
INDIANAPOLIS, IN 46256            510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: TINA-QUANT APOLIPOPROTEIN A-1 VER.2
ROCHE DIAGNOSTICS CORP.           510(k) NO: K013278(TRADITIONAL)
ATTN: HELEN  TORNEY               PHONE NO : 317-521-7643
9115 HAGUE ROAD                   SE DECISION MADE: 15-NOV-01
INDIANAPOLIS, IN 46256            510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: OMNI C ANALYZER
ROCHE DIAGNOSTICS CORP.           510(k) NO: K013373(SPECIAL)
ATTN: JENNIFER  TRIBETT           PHONE NO : 800-428-5074
9115 HAGUE RD.                    SE DECISION MADE: 02-NOV-01
INDIANAPOLIS, IN 46250            510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: RUSCH BRONCHUS BLOCKER KIT
RUSCH INTL.                       510(k) NO: K010596(TRADITIONAL)
ATTN: KARENANN J BROZOWSKI        PHONE NO : 603-532-7706
50 PLANTATION DRIVE               SE DECISION MADE: 21-NOV-01
JAFFERY, NH 03452                 510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: RUSCH PERCUTANEOUS NEPHROSTOMY CATHETER SETS
RUSCH INTL.                       510(k) NO: K011121(TRADITIONAL)
ATTN: JULIE A BEAUMONT            PHONE NO : 603-532-0204
50 PLANTATION DRIVE               SE DECISION MADE: 16-NOV-01
JAFFERY, NH 03452                 510(k) SUMMARY AVAILABLE FROM FDA

 
DEVICE: BALLPEN SPINAL NEEDLE W/WO INTRODUCER
RUSCH INTL.                       510(k) NO: K011122(TRADITIONAL)
ATTN: JULIE A BEAUMONT            PHONE NO : 603-532-0204
50 PLANTATION DRIVE               SE DECISION MADE: 16-NOV-01
JAFFERY, NH 03452                 510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: RUSCH POLYFLEX STENT KIT
RUSCH INTL.                       510(k) NO: K013266(TRADITIONAL)
ATTN: KARENANN J BROZOWSKI        PHONE NO : 603-532-0203
50 PLANTATION DRIVE               SE DECISION MADE: 27-NOV-01
JAFFERY, NH 03452                 510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: S & C HYDRO VINYL POLYSILOXANE IMPRESSION MATERIAL
S & C POLYMER GMBH                510(k) NO: K012767(TRADITIONAL)
ATTN: CHRISTIAN  BOTTCHER         PHONE NO : 49 412 18619
ROBERT-BOSCH-STRABE 5             SE DECISION MADE: 01-NOV-01
ELMSHORN, GERMANY D-25335         510(k) STATEMENT

DEVICE: ISOBAR SPINAL SYSTEM
SCIENT'X                          510(k) NO: K013440(SPECIAL)
ATTN: JOANNA  DROEGE              PHONE NO : 512-832-9500
9800 METRIC BLVD.                 SE DECISION MADE: 16-NOV-01
AUSTIN, TX 78758                  510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: ISOBAR SPINAL SYSTEM
SCIENT'X                          510(k) NO: K013444(SPECIAL)
ATTN: JOANNA  DROEGE              PHONE NO : 512-832-9500
9800 METRIC BLVD.                 SE DECISION MADE: 16-NOV-01
AUSTIN, TX 78758                  510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: SCITON IMAGE HAIR REMOVAL LASER
SCITON, INC.                      510(k) NO: K012552(TRADITIONAL)
ATTN: PETER N ALLEN               PHONE NO : 650-493-9155
845 COMMERCIAL STREET             SE DECISION MADE: 05-NOV-01
PALO ALTO, CA 94303               510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: OPTIMA URS UNIVERSAL RADIOGRAPHIC SYSTEM
SEDECAL USA, , INC.               510(k) NO: K012546(TRADITIONAL)
ATTN: DANIEL  KAMM                PHONE NO : 847-374-1727
P.O. BOX 7007                     SE DECISION MADE: 02-NOV-01
DEERFIELD, IL 60015               510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: SEMPERMED DERMA PLUS, SIZES 5.5,6,6.5,7,7.5,8,8.5,9
SEMPERIT TECHNISCHE PRODUKTE GESEL510(k) NO: K012819(ABBREVIATED)
ATTN: JAY  MANSOUR                PHONE NO : 678-908-8180
1308 MORNINGSTAR PARK DR          SE DECISION MADE: 16-NOV-01
APHARETTA, GA 30022               510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: SERIM BLOOD LEAK TEST STRIP-2
SERIM RESEARCH CORP.              510(k) NO: K012115(TRADITIONAL)
ATTN: PATRICA  RUPCHOCK           PHONE NO : 219-264-3440
P.O. BOX 4002                     SE DECISION MADE: 30-NOV-01
ELKHART, IN 46514-0002            510(k) SUMMARY AVAILABLE FROM FDA

 
DEVICE: MOTEX NITRILE EXAMINATION GLOVES POWDER-FREE
SHANGHAI MOTEX HEALTHCARE CO., LTD510(k) NO: K013261(TRADITIONAL)
ATTN: TONY T K CHENG              PHONE NO : 862 159 799888
NO. 6318, FANG HUANG RD.,         SE DECISION MADE: 29-NOV-01
HUAXIN                            510(k) SUMMARY AVAILABLE FROM FDA
QINGPU, SHANGHAI, CHINA           THIRD PARTY REVIEW

DEVICE: SNAZZY2
SHOPRIDER INTL., INC.             510(k) NO: K011473(TRADITIONAL)
ATTN: CHRIS  TINSLEY              PHONE NO : 162 032 52629
169 KEN TZU, SHANG KEN VILLAGE    SE DECISION MADE: 16-NOV-01
HSIN FENG                         510(k) STATEMENT
HSIANG, HSINCHU COUNTY, CHINA (TAIWAN)

DEVICE: SOMATOM P30 CT SYSTEMS
SIEMENS MEDICAL SYSTEMS, INC.     510(k) NO: K013522(TRADITIONAL)
ATTN: PRAVEEN  NADKARNI           PHONE NO : 732-321-4950
186 WOOD AVENUE SOUTH             SE DECISION MADE: 07-NOV-01
ISELIN, NJ 08830                  510(k) SUMMARY AVAILABLE FROM FDA
                                  THIRD PARTY REVIEW

DEVICE: SIGMA DIAGNOSTICS AUTO D-DIMER CONTROL, LEVEL 2, MODEL A8096
SIGMA DIAGNOSTICS, INC.           510(k) NO: K013544(TRADITIONAL)
ATTN: WILLIAM R GILBERT II        PHONE NO : 314-286-6693
545 SOUTH EWING AVE.              SE DECISION MADE: 15-NOV-01
ST. LOUIS, MO 63103               510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: SIGMA DIAGNOSTICS AUTO D-DIMER CONTROL, LEVEL 3, MODEL A8221
SIGMA DIAGNOSTICS, INC.           510(k) NO: K013545(TRADITIONAL)
ATTN: WILLIAM R GILBERT II        PHONE NO : 314-286-6693
545 SOUTH EWING AVE.              SE DECISION MADE: 15-NOV-01
ST. LOUIS, MO 63103               510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: SILMED NASAL SEPTAL BUTTON
SILMED INCORPORATED               510(k) NO: K013696(TRADITIONAL)
ATTN: RAMA  GUNDLAPALLI           PHONE NO : 219-453-3877
3987 LAKEVIEW TRAIL               SE DECISION MADE: 28-NOV-01
LEESBURG,, IN 46538               510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: CEREC INLAB AND CEREC SCAN
SIRONA DENTAL SYSTEMS GMBH        510(k) NO: K012517(TRADITIONAL)
ATTN: SHEILA  HEMEON-HEYER        PHONE NO : 508-643-0434
49 PLAIN STREET                   SE DECISION MADE: 01-NOV-01
NORTH ATTLEBORO, MA 02760-4153    510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: MINIME NASAL MASK, MODEL P/N 50220
SLEEPNET CORP.                    510(k) NO: K013306(SPECIAL)
ATTN: PAUL R CHIESA               PHONE NO : 603-624-1911
1050 PERIMETER RD.,               SE DECISION MADE: 02-NOV-01
LOCKHEED AIR CENTER               510(k) STATEMENT
MANCHESTER, NH 03103

 
DEVICE: SMART GLOVE STERILE NITRILE EXAM GLOVE
SMART GLOVE CORP. SDN BHD         510(k) NO: K012853(TRADITIONAL)
ATTN: NG YEW  SOON                PHONE NO : 603 329 16100
LOT 6487 BATU 5 3/4               SE DECISION MADE: 16-NOV-01
JALAN KAPAR                       510(k) STATEMENT
KLANG SELANGOR, MALAYSIA 42100

DEVICE: STERILE LATEX EXAMINATION GLOVES (POWDERED) WITH PROTEIN CLAIM L
SMART GLOVE CORP. SDN BHD         510(k) NO: K012856(TRADITIONAL)
ATTN: FOO  KHON PU                PHONE NO : 603 329 17526
LOT 6487 BATU 5 3/4               SE DECISION MADE: 16-NOV-01
JALAN KAPAR                       510(k) STATEMENT
KLANG SELANGOR, MALAYSIA 42100

DEVICE: SMITH & NEPHEW PHOENIX 5.0 ALLOGRAFT ANCHOR KIT
SMITH & NEPHEW, INC.              510(k) NO: K011985(TRADITIONAL)
ATTN: TIM  CRABTREE               PHONE NO : 978-749-1068
160 DASCOMB RD.                   SE DECISION MADE: 02-NOV-01
ANDOVER, MA 01810                 510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: SMITH & NEPHEW VASCULAR VIDEOENDOSCOPE SYSTEM, MODEL 7209273
SMITH & NEPHEW, INC.              510(k) NO: K012724(TRADITIONAL)
ATTN: JANICE  HASELTON            PHONE NO : 978-749-1494
160 DASCOMB RD.                   SE DECISION MADE: 08-NOV-01
ANDOVER, MA 01810                 510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: TORIC EYE-Q (XYLOFILCON A) SOFT (HYDROPHILIC) TORIC MULTIFOCAL C
SOFLEX CONTACT LENS INDUSTRIES LTD510(k) NO: K013467(TRADITIONAL)
ATTN: KEVIN  WALLS                PHONE NO : 720-962-5412
13 RED FOX LANE                   SE DECISION MADE: 20-NOV-01
LITTLETON, CO 80127               510(k) STATEMENT

DEVICE: EYE-Q (XYLOFILCON A) SOFT (HYDROPHILIC) MULTIFOCAL CONTACT LENS
SOFLEX CONTACT LENS INDUSTRIES LTD510(k) NO: K013469(TRADITIONAL)
ATTN: KEVIN  WALLS                PHONE NO : 720-962-5412
13 RED FOX LANE                   SE DECISION MADE: 20-NOV-01
LITTLETON, CO 80127               510(k) STATEMENT

DEVICE: CORRESTORE PATCH, MODELS 1.5P2, 2P3, 3P4; CORRESTORE SIZER, MODE
SOMANETICS CORP.                  510(k) NO: K011487(TRADITIONAL)
ATTN: RONALD A WIDMAN             PHONE NO : 248-689-3050
1653 EAST MAPLE RD.               SE DECISION MADE: 21-NOV-01
TROY, MI 48083-4208               510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: SCANTAC MEMBRANE OR SCANTAC STRIP
SONOTECH, INC.                    510(k) NO: K013170(TRADITIONAL)
ATTN: MARGARET J LARSON           PHONE NO : 360-671-9024
774 MARINE DR.                    SE DECISION MADE: 13-NOV-01
BELLINGHAM, WA 98225              510(k) STATEMENT

DEVICE: SORING GMBH SONOCA 180/190
SORING GMBH MEDIZINTECHNIK        510(k) NO: K012753(TRADITIONAL)
ATTN: CARL  ALLETTO               PHONE NO : 214-262-4209
1100 LAKEVIEW BLVD.               SE DECISION MADE: 13-NOV-01
DENTON, TX 76208                  510(k) SUMMARY AVAILABLE FROM FDA

 
DEVICE: LIFTLOC SAFETY INFUSION SET
SPECIALIZED HEALTH PRODUCTS, INC. 510(k) NO: K013394(TRADITIONAL)
ATTN: MARK  NELSON                PHONE NO : 801-298-3360
585 WEST 500 SOUTH                SE DECISION MADE: 08-NOV-01
BOUNTIFUL, UT 84010               510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: C3 ANTERIOR CERVICAL PLATE SYSTEM
SPINE VISION, INC                 510(k) NO: K012881(TRADITIONAL)
ATTN: DAVID W MULLIS, JR          PHONE NO : 770-207-9174
BOX 39 367 PLEASANT VALLEY RD     SE DECISION MADE: 26-NOV-01
GOOD HOPE, GA 30641               510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: STERILE POWDER-FREE LATEX SURGICAL GLOVES
SSN GLOVES (M) SDN BHD            510(k) NO: K012880(TRADITIONAL)
ATTN: CLINTON A TECK LEONG        PHONE NO : 603 778 12829
NO. 1, JALAN 203, OFF JALAN       SE DECISION MADE: 16-NOV-01
TANDANG                           510(k) STATEMENT
PETALING, JALA SELANGOR, MALAYSIA 46050

DEVICE: STERILE POWDERED LATEX SURGICAL GLOVES
SSN GLOVES (M) SDN BHD            510(k) NO: K012896(TRADITIONAL)
ATTN: CLINTON A TECK LEONG        PHONE NO : 603 778 12829
NO. 1, JALAN 203, OFF JALAN       SE DECISION MADE: 16-NOV-01
TANDANG                           510(k) STATEMENT
PETALING, JALA SELANGOR, MALAYSIA 46050

DEVICE: STANDARD IMAGING IVB 1000 WELL CHAMBER
STANDARD IMAGING, INC.            510(k) NO: K013548(SPECIAL)
ATTN: RAYMOND  RIDDLE             PHONE NO : 608-831-0025
7601 MURPHY DRIVE                 SE DECISION MADE: 09-NOV-01
MIDDLETON, WI 53562-2766          510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: REPROCESSED POWERED  ARTHROSCOPIC ACCESSORIES
STERILMED, INC.                   510(k) NO: K012536(TRADITIONAL)
ATTN: PATRICK  FLEISCHHACKER      PHONE NO : 888-856-4870
11400 73RD AVE. NORTH             SE DECISION MADE: 02-NOV-01
MAPLE GROVE, MN 55369             510(k) STATEMENT

DEVICE: REPROCESSED HARMONIC
STERILMED, INC.                   510(k) NO: K012571(TRADITIONAL)
ATTN: PATRICK  FLEISCHHACKER      PHONE NO : 763-488-3400
11400 73RD AVE. NORTH             SE DECISION MADE: 07-NOV-01
MAPLE GROVE, MN 55369             510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: REPROCESSED ENDOSCOPIC TROCAR
STERILMED, INC.                   510(k) NO: K012578(TRADITIONAL)
ATTN: PATRICK  FLEISCHHACKER      PHONE NO : 763-488-3400
11400 73RD AVE N., SUITE 100      SE DECISION MADE: 07-NOV-01
MAPLE GROVE, MN 55369             510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: REPROCESSED PHACO TIPS
STERILMED, INC.                   510(k) NO: K012579(TRADITIONAL)
ATTN: PATRICK  FLEISCHHACKER      PHONE NO : 763-488-3400
11400 73RD AVE N., SUITE 100      SE DECISION MADE: 08-NOV-01
MAPLE GROVE, MN 55369             510(k) SUMMARY AVAILABLE FROM FDA

 
DEVICE: REPROCESSED LAPAROSCOPIC ELECTRIC INSTUMENTS
STERILMED, INC.                   510(k) NO: K012598(TRADITIONAL)
ATTN: PATRICK F FLEISCHHACKER     PHONE NO : 763-488-3400
11400 73RD AVE. NORTH             SE DECISION MADE: 07-NOV-01
MAPLE GROVE, MN 55369             510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: REPROCESSED RF ARTHROSCOPY PROBES
STERILMED, INC.                   510(k) NO: K012679(TRADITIONAL)
ATTN: PATRICK  FLEISCHHACKER      PHONE NO : 888-856-4870
11400 73RD AVE. NORTH             SE DECISION MADE: 08-NOV-01
MAPLE GROVE, MN 55369             510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: REPROCESSED LASER PROBE
STERILMED, INC.                   510(k) NO: K012682(TRADITIONAL)
ATTN: PATRICK  FLEISCHHACKER      PHONE NO : 888-856-4870
11400 73RD AVE. NORTH             SE DECISION MADE: 08-NOV-01
MAPLE GROVE, MN 55369             510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: REPROCESSED LIGHT PIPES
STERILMED, INC.                   510(k) NO: K012683(TRADITIONAL)
ATTN: PATRICK  FLEISCHHACKER      PHONE NO : 888-856-4870
11400 73RD AVE. NORTH             SE DECISION MADE: 08-NOV-01
MAPLE GROVE, MN 55369             510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: EVERSTICK
STICK TECH LTD.                   510(k) NO: K011788(TRADITIONAL)
ATTN: WILLIAM M TROETEL           PHONE NO : 914-664-1640
80 PARKWAY WEST                   SE DECISION MADE: 05-NOV-01
MOUNT VERNON, NY 10552            510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: EVERSTICKNET
STICK TECH LTD.                   510(k) NO: K011799(TRADITIONAL)
ATTN: WILLIAM M TROETEL           PHONE NO : 914-664-1640
80 PARKWAY WEST                   SE DECISION MADE: 05-NOV-01
MOUNT VERNON, NY 10552            510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: SICKLE-CHEX
STRECK LABORATORIES, INC.         510(k) NO: K013316(TRADITIONAL)
ATTN: PAUL  KITTELSON             PHONE NO : 402-537-5312
7002 SOUTH 109TH ST.              SE DECISION MADE: 06-NOV-01
LA VISTA, NE 68128                510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: NEPTUNE WASTE MANAGEMENT STSTEM
STRYKER INSTRUMENTS               510(k) NO: K012991(TRADITIONAL)
ATTN: SUZANNE  VELAZQUEZ          PHONE NO : 616-323-7700
4100 EAST MILHAM AVE.             SE DECISION MADE: 29-NOV-01
KALAMAZOO, MI 49001               510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: SCREW VENT IMPLANT; TAPERED SCREW VENT IMPLANT
SULZER DENTAL, INC.               510(k) NO: K013227()
ATTN: FOSTER  BOOP                PHONE NO : 760-929-4300
1900 ASTON AVE.                   SE DECISION MADE: 19-NOV-01
CARLSBAD, CA 92008-7308           510(k) SUMMARY AVAILABLE FROM FDA

 
DEVICE: CONVERGE ACETABULAR SYSTEM
SULZER ORTHOPEDICS, INC.          510(k) NO: K012739(TRADITIONAL)
ATTN: MITCHELL A DHORITY          PHONE NO : 512-432-9202
9900 SPECTRUM DR.                 SE DECISION MADE: 14-NOV-01
AUSTIN, TX 78717                  510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: PRIZM BLADE (MORIA MODEL) LSK / MK8510LSK; PRIZM BLADE (MORIA MO
SURGIN SURGICAL INSTRUMENTATION, I510(k) NO: K011195(TRADITIONAL)
ATTN: DON  HAAR                   PHONE NO : 714-832-6300
14762 BENTLEY CIRCLE              SE DECISION MADE: 06-NOV-01
TUSTIN, CA 92680                  510(k) STATEMENT

DEVICE: CAPIOX RX HARDSHELL RESERVOIR
TERUMO CARDIOVASCULAR SYSTEMS CORP510(k) NO: K013526(SPECIAL)
ATTN: GARRY A COURTNEY            PHONE NO : 800-283-7866
125 BLUE BALL ROAD                SE DECISION MADE: 15-NOV-01
ELKTON, MD 21921                  510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: CAROTID GUIDING SHEATH
TERUMO MEDICAL CORP.              510(k) NO: K012812(TRADITIONAL)
ATTN: YUK-TING  LEWIS             PHONE NO : 410-392-7213
950 ELKTON BLVD.                  SE DECISION MADE: 14-NOV-01
ELKTON, MD 21921                  510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: RENAL GUIDING SHEATH
TERUMO MEDICAL CORP.              510(k) NO: K012854(TRADITIONAL)
ATTN: YUK-TING  LEWIS             PHONE NO : 410-392-7213
125 BLUE BALL ROAD                SE DECISION MADE: 21-NOV-01
ELKTON, MD 21921                  510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: CLIRANS E-SERIES DIALYZER
TERUMO MEDICAL CORP.              510(k) NO: K013550(SPECIAL)
ATTN: SANDI  HARTKA               PHONE NO : 410-392-7243
125 BLUE BALL ROAD                SE DECISION MADE: 20-NOV-01
ELKTON, MD 21921                  510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: BITEM ANGEL RELINE KIT, BITEM LABORATORY KIT, MODELS 120110, 120
THERMOELASTIC TECHNOLOGIES, INC.  510(k) NO: K012882(TRADITIONAL)
ATTN: ART  WARD                   PHONE NO : 813-645-2855
962 ALLEGRO LANE                  SE DECISION MADE: 14-NOV-01
APOLLO BEACH, FL 33572            510(k) STATEMENT

DEVICE: HPI SENSI GRIP STERILE POWDERED LATEX SURGICAL GLOVE,WITH LABELE
TILLOTSON HEALTHCARE CORP.        510(k) NO: K013324(TRADITIONAL)
ATTN: F.W.  PERRELLA              PHONE NO : 603-472-6600
360 ROUTE 101 W                   SE DECISION MADE: 29-NOV-01
BEDFORD, NH 03110                 510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: DIGITAL RADIOGRAPHY SYSTEM, MODEL DFP-8000D
TOSHIBA AMERICA MEDICAL SYSTEMS, I510(k) NO: K013608(TRADITIONAL)
ATTN: DIANA  THORSON              PHONE NO : 714-730-5000
2441 MICHELLE DR.                 SE DECISION MADE: 15-NOV-01
P.O. BOX 2068                     510(k) SUMMARY AVAILABLE FROM FDA
TUSTIN, CA 92781-2068             THIRD PARTY REVIEW

 
DEVICE: SSA-770A, APLIO ULTRASOUND SYSTEM
TOSHIBA AMERICA MEDICAL SYSTEMS, I510(k) NO: K013633(TRADITIONAL)
ATTN: PAUL  BIGGINS               PHONE NO : 714-730-5000
2441 MICHELLE DR.                 SE DECISION MADE: 13-NOV-01
P.O. BOX 2068                     510(k) SUMMARY AVAILABLE FROM FDA
TUSTIN, CA 92781-2068             THIRD PARTY REVIEW

DEVICE: SENSITITRE HAEMOPHILUS/STREPTOCOCCUS PNEUMONIAE (HP) MIC PLATE
TREK DIAGNOSTIC SYSTEMS, INC.     510(k) NO: K012921(TRADITIONAL)
ATTN: CYNTHIA C KNAPP             PHONE NO : 800-216-9036
29299 CLEMENS RD., SUITE 1-K      SE DECISION MADE: 02-NOV-01
WESTLAKE, OH 44145                510(k) STATEMENT

DEVICE: SENSITITRE HAEMOPHILUS/STREPTOCOCCUS PNEUMONIAE (HP) MIC PLATE
TREK DIAGNOSTIC SYSTEMS, INC.     510(k) NO: K013075(TRADITIONAL)
ATTN: CYNTHIA C KNAPP             PHONE NO : 800-216-9036
29299 CLEMENS RD. SUITE 1-K       SE DECISION MADE: 26-NOV-01
WESTLAKE, OH 44145                510(k) STATEMENT

DEVICE: HAEMOPHILUS/STREPTOCOCCUS PNEUMONIAE (HP)MIC SUSCEPTIBILITY PLAT
TREK DIAGNOSTIC SYSTEMS, INC.     510(k) NO: K013195(TRADITIONAL)
ATTN: CYNTHIA C KNAPP             PHONE NO : 800-216-9036
29299 CLEMENS RD., SUITE 1-K      SE DECISION MADE: 07-NOV-01
WESTLAKE, OH 44145                510(k) STATEMENT

DEVICE: HAEMOPHILUS/STREPTOCOCCUS PNEUMONIAE (HP) MIC PLATE
TREK DIAGNOSTIC SYSTEMS, INC.     510(k) NO: K013368(TRADITIONAL)
ATTN: CYNTHIA C KNAPP             PHONE NO : 800-216-9036
29299 CLEMENS RD., SUITE 1-K      SE DECISION MADE: 20-NOV-01
WESTLAKE, OH 44145                510(k) STATEMENT

DEVICE: HELICAL COMPRESSION ANCHOR SYSTEM, NON-CANNULATED
TRIAGE MEDICAL INC                510(k) NO: K012817(TRADITIONAL)
ATTN: GREG  HOLLAND               PHONE NO : 949-262-0411
3722 AVE. SAUSALITO               SE DECISION MADE: 20-NOV-01
IRVINE, CA 92606                  510(k) STATEMENT

DEVICE: HELICAL COMPRESSION ANCHOR SYSTEM, CANNULATED SINGLE HELIX
TRIAGE MEDICAL INC                510(k) NO: K012818(TRADITIONAL)
ATTN: GREG H HOLLAND              PHONE NO : 949-262-0411
3722 AVE. SAUSALITO               SE DECISION MADE: 20-NOV-01
IRVINE, CA 92606                  510(k) STATEMENT

DEVICE: UNI-GOLD STREP A TEST KIT
TRINITY BIOTECH, PLC              510(k) NO: K011709(TRADITIONAL)
ATTN: FIONA  CAMPBELL             PHONE NO : 011 353 12769800
IDA BUSINESS PARK                 SE DECISION MADE: 08-NOV-01
BRAY, IRELAND                     510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: ORALLITE COMPREHENSIVE EXAM TRAY
TRYLON CORP.                      510(k) NO: K012070(TRADITIONAL)
ATTN: MARTIN L LONKY              PHONE NO : 310-327-8820
970 WEST 190TH ST., SUITE 850     SE DECISION MADE: 27-NOV-01
TORRANCE, CA 90502-1037           510(k) STATEMENT

 
DEVICE: CLEARBLUE EASY EARLY RESULT PREGNANCY TEST
UNIPATH LTD.                      510(k) NO: K013372(SPECIAL)
ATTN: STEVEN H ARMSTRONG          PHONE NO : 212-418-8515
390 PARK AVENUE                   SE DECISION MADE: 09-NOV-01
NEW YORK, NY 10022-4698           510(k) STATEMENT

DEVICE: VT-1
V.T.S.,INC.                       510(k) NO: K012619(TRADITIONAL)
ATTN: DENNIS L BELL               PHONE NO : 866-344-6044
701 S. MAIN                       SE DECISION MADE: 09-NOV-01
NEWKIRK, OK 74647                 510(k) STATEMENT

DEVICE: SE-200
V.T.S.,INC.                       510(k) NO: K012620(TRADITIONAL)
ATTN: DENNIS L BELL               PHONE NO : 866-344-6044
701 S. MAIN                       SE DECISION MADE: 09-NOV-01
NEWKIRK, OK 74647                 510(k) STATEMENT

DEVICE: VANGUARD REPROCESSED PHACOEMULSIFICATION
VANGUARD MEDICAL CONCEPTS, INC.   510(k) NO: K012698(TRADITIONAL)
ATTN: MIKE  SAMMON                PHONE NO : 863-683-8680
5307 GREAT OAK DR.                SE DECISION MADE: 09-NOV-01
LAKELAND, FL 33815                510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: VANGUARD REPROCESSED ENDOSCOPIC INSTRUMENTS
VANGUARD MEDICAL CONCEPTS, INC.   510(k) NO: K012700(TRADITIONAL)
ATTN: MIKE  SAMMON                PHONE NO : 863-683-8680
5307 GREAT OAK DR.                SE DECISION MADE: 07-NOV-01
LAKELAND, FL 33815                510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: VASCULAR ARCHITECTS ASPIRE COVERED STENT AND CONTROLLED EXPANSIO
VASCULAR ARCHITECTS, INC.         510(k) NO: K012544(TRADITIONAL)
ATTN: JEAN M CAILLOUETTE          PHONE NO : 408-392-7437
1830 BERING DR.                   SE DECISION MADE: 15-NOV-01
SAN JOSE, CA 95112-4226           510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: SE-300 VACUUM THERAPY SYSTEM
VTS, INC.                         510(k) NO: K012639(TRADITIONAL)
ATTN: DENNIS L BELL               PHONE NO : 866-344-6044
701 S. MAIN STREET                SE DECISION MADE: 09-NOV-01
NEWKIRK, OK 74647                 510(k) STATEMENT

DEVICE: SE-100 VACUUM ERECTION DEVICE
VTS, INC.                         510(k) NO: K012662(TRADITIONAL)
ATTN: DENNIS L BELL               PHONE NO : 866-344-6044
701 S. MAIN STREET                SE DECISION MADE: 09-NOV-01
NEWKIRK, OK 74647                 510(k) STATEMENT

DEVICE: CARDIOVASCULAR ARRAY
W.L. GORE & ASSOCIATES,INC        510(k) NO: K013810(TRADITIONAL)
ATTN: TRACEY D WOLF               PHONE NO : 302-292-4720
1901 BARKSDALE ROAD               SE DECISION MADE: 27-NOV-01
NEWARK, DE 19714                  510(k) SUMMARY AVAILABLE FROM FDA
                                  THIRD PARTY REVIEW

 
DEVICE: W.O.M. LASER U100
W.O.M. WORLD OF MEDICINE, GMBH    510(k) NO: K011175(TRADITIONAL)
ATTN: MICHAEL  MCGRAIL            PHONE NO : 617-868-3995
91 TROWBRIDGE STREET              SE DECISION MADE: 01-NOV-01
# 21                              510(k) SUMMARY AVAILABLE FROM FDA
CAMBRIDGE, MA 02138

DEVICE: LACTOSORB CRANIOFACIAL ANCHOR-PUSH SCREW
WALTER LORENZ SURGICAL, INC.      510(k) NO: K013557(SPECIAL)
ATTN: TRACY J BICKEL              PHONE NO : 219-267-6639
P.O. BOX 587                      SE DECISION MADE: 16-NOV-01
WARSAW,, IN 46581-0578            510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: BIOPORTA G, MODEL 2052
WIELAND EDELMETALLE GMBH & CO.    510(k) NO: K012826(TRADITIONAL)
ATTN: GERHARD  POLZER             PHONE NO : 497 231 3705219
SCHWENNINGER STRABE 13            SE DECISION MADE: 01-NOV-01
PFORZHEIM, GERMANY D-75179        510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: PORTA AURIUM, MODEL 2067
WIELAND EDELMETALLE GMBH & CO.    510(k) NO: K012827(TRADITIONAL)
ATTN: GERHARD  POLZER             PHONE NO : 497 231 3705219
SCHWENNINGER STRABE 13            SE DECISION MADE: 01-NOV-01
PFORZHEIM, GERMANY D-75179        510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: PORTA SMK 82, MODEL 2032
WIELAND EDELMETALLE GMBH & CO.    510(k) NO: K012828(TRADITIONAL)
ATTN: GERHARD  POLZER             PHONE NO : 497 231 3705219
SCHWENNINGER STRABE 13            SE DECISION MADE: 01-NOV-01
D-75179 PFORZHEIM, GERMANY        510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: BIO PORTADUR, ORDER-NO.:2017
WIELAND EDELMETALLE GMBH & CO.    510(k) NO: K012831(TRADITIONAL)
ATTN: GERHARD  POLZER             PHONE NO : 497 231 3705219
SCHWENNINGER STRABE 13            SE DECISION MADE: 01-NOV-01
PFORZHEIM, GERMANY D-75179        510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: PORTA GEO TI MODEL #2004
WIELAND EDELMETALLE GMBH & CO.    510(k) NO: K012834(TRADITIONAL)
ATTN: GEHARD  POLZER              PHONE NO : 497 231 3705219
SCHWENNINGER STRABE 13            SE DECISION MADE: 01-NOV-01
D-75179 PFORZHEIM, GERMANY        510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: PORTA MAXIMUM, MODEL# 2066
WIELAND EDELMETALLE GMBH & CO.    510(k) NO: K012835(TRADITIONAL)
ATTN: GERHARD  POLZER             PHONE NO : 497 231 3705219
SCHWENNINGER STRABE 13            SE DECISION MADE: 01-NOV-01
D-75179 PFORZHEIM, GERMANY        510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: DUO PAL 6, ORDER-NO.: 2154
WIELAND EDELMETALLE GMBH & CO.    510(k) NO: K012841(TRADITIONAL)
ATTN: GERHARD  POLZER             PHONE NO : 49 723 13705219
SCHWENNINGER STRABE 13            SE DECISION MADE: 20-NOV-01
PFORZHEIM, GERMANY D-75179        510(k) SUMMARY AVAILABLE FROM FDA

 
DEVICE: PORTADUR P 2, MODEL #2031
WIELAND EDELMETALLE GMBH & CO.    510(k) NO: K012843(TRADITIONAL)
ATTN: GEHARD  POLZER              PHONE NO : 497 231 3705219
SCHWENNINGER STRABE 13            SE DECISION MADE: 02-NOV-01
D-75179 PFORZHEIM, GERMANY        510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: WIENER LAB.MG-COLOR AA, MODEL 2X50 ML CAT. N 1580001
WIENER LABORATORIES S.A.I.C.      510(k) NO: K012326(TRADITIONAL)
ATTN: VIVIANA  CETOLA             PHONE NO : 543 414 329191
2944 RIOBAMBA                     SE DECISION MADE: 08-NOV-01
ROSARIO, ARGENTINA 2000           510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: WIENER LAB.FOSFATEMIA UV, MODELS 1X100 ML CAT.N 1382321, 4X20 ML
WIENER LABORATORIES S.A.I.C.      510(k) NO: K013095(TRADITIONAL)
ATTN: VIVIANA  CETOLA             PHONE NO : 543 414 851982
2944 RIOBAMBA                     SE DECISION MADE: 16-NOV-01
ROSARIO, ARGENTINA 2000           510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: WIENER LAB.FER-COLOR AA, MODEL 5X 20 ML CAT.N 1492003
WIENER LABORATORIES S.A.I.C.      510(k) NO: K013097(TRADITIONAL)
ATTN: VIVIANA  CETOLA             PHONE NO : 543 414 851982
2944 RIOBAMBA                     SE DECISION MADE: 13-NOV-01
ROSARIO, ARGENTINA 2000           510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: WIENER LAB. AMILASA 405 CINETICA AA, WIENER LAB.AMILASA 405 CINE
WIENER LABORATORIES S.A.I.C.      510(k) NO: K013101(TRADITIONAL)
ATTN: VIVIANA  CETOLA             PHONE NO : 543 414 329191
2944 RIOBAMBA                     SE DECISION MADE: 16-NOV-01
ROSARIO, ARGENTINA 2000           510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: WIENER LAB. FER-COLOR TRANSFERRINA, MODEL AUX. REAGENTS FOR 25 S
WIENER LABORATORIES S.A.I.C.      510(k) NO: K013102(TRADITIONAL)
ATTN: VIVIANA  CETOLA             PHONE NO : 543 414 851982
2944 RIOBAMBA                     SE DECISION MADE: 13-NOV-01
ROSARIO, ARGENTINA 2000           510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: WIENER LAB. GOT (AST) UV AA. WEINER LAB. GOT (AST) UV UNITEST, M
WIENER LABORATORIES S.A.I.C.      510(k) NO: K013145(TRADITIONAL)
ATTN: VIVIANA  CETOLA             PHONE NO : 543 414 329191
2944 RIOBAMBA                     SE DECISION MADE: 27-NOV-01
ROSARIO, ARGENTINA 2000           510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: SEREINE EXTRA STRENGTH DAILY CLEANER
WILSA, INC.                       510(k) NO: K011561(TRADITIONAL)
ATTN: SALLY  COOK                 PHONE NO : 303-936-1137
2172 SOUTH JASON ST.              SE DECISION MADE: 20-NOV-01
DENVER, CO 80223                  510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: ADVANCE UNICONDYLAR KNEE SYSTEM
WRIGHT MEDICAL TECHNOLOGY, INC.   510(k) NO: K012591(ABBREVIATED)
ATTN: EHAB M ESMAIL               PHONE NO : 901-867-4732
5677 AIRLINE RD.                  SE DECISION MADE: 02-NOV-01
ARLINGTON, TN 38002               510(k) SUMMARY AVAILABLE FROM FDA

 
DEVICE: DEVICE MODIFICATION OF ENTERAL FEEDING SETS FOR GRAVITY AND PUMP
ZEVEX, INC.                       510(k) NO: K012147(SPECIAL)
ATTN: SUSAN P SCHMIDT             PHONE NO : 801-264-1001
4314 ZEVEX PARK LN.               SE DECISION MADE: 02-NOV-01
SALT LAKE CITY, UT 84123          510(k) SUMMARY AVAILABLE FROM FDA


 
                                                TOTAL 510(k)s THIS PERIOD   313
                                                TOTAL WITH SUMMARIES        249
                                                TOTAL WITH STATEMENTS        64
    
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