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Medical Devices

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July 2003 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-JUL-2003 THROUGH 31-JUL-2003

 
DEVICE: STEREOTACTIC BODY FRAME, MODEL COD. 70-1A
3D LINE USA, INC.                 510(k) NO: K031631(TRADITIONAL)
ATTN: NADER  SALEHI               PHONE NO : 410-581-6701
11419 CROWNRIDGE RD., STE.15      SE DECISION MADE: 18-JUL-03
OWINGS MILLS, MD 21117            510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: C-REACTIVE PROTEIN (CRP)
ABBOTT LABORATORIES               510(k) NO: K030899(TRADITIONAL)
ATTN: LINDA  MORRIS               PHONE NO : 972-518-6711
1920 HURD DR.                     SE DECISION MADE: 02-JUL-03
IRVING, TX 75038                  510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: ECN ELECTRONIC VIDEO CYSTONEPHROSCOPE
ACMI CORPORATION                  510(k) NO: K030960(TRADITIONAL)
ATTN: JOHN  DELUCIA               PHONE NO : 508-804-2617
136 TURNPIKE RD.                  SE DECISION MADE: 16-JUL-03
SOUTHBOROUGH, MA 01772            510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: ACON STREP A RAPID TEST DEVICE
ACON LABORATORIES, INC.           510(k) NO: K031784(SPECIAL)
ATTN: EDWARD  TUNG                PHONE NO : 858-535-2038
4108 SORRENTO VALLEY BLVD.        SE DECISION MADE: 14-JUL-03
SAN DIEGO, CA 92121               510(k) STATEMENT

DEVICE: DIGITAL CLINICAL THERMOMETER, MODELS ACT2130, ACT 2230, ACT 2330
ACTHERM, INC.                     510(k) NO: K031905(SPECIAL)
ATTN: RICHARD  HSIEH              PHONE NO : 886 3 5537315
6TH F, NO 85                      SE DECISION MADE: 07-JUL-03
KUAN-MIN 6 ROAD JUBEI 302         510(k) STATEMENT
HSINCHU, CHINA (TAIWAN) 302

DEVICE: ACUMED SMALL BONE LOCKING ROD SYSTEM II
ACUMED LLC                        510(k) NO: K031438(TRADITIONAL)
ATTN: ED  BOEHMER                 PHONE NO : 503-627-9957
5885 NW CORNELIUS PASS RD.        SE DECISION MADE: 17-JUL-03
HILLSBORO, OR 97124-9432          510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: "FAST THROW" STAINLESS STEEL SURGICAL SUTURE
ADVANCED SURGICAL PRODUCTS, INC.  510(k) NO: K030926(TRADITIONAL)
ATTN: JEFFERY S JONES             PHONE NO : 650-207-6987
681 MANZANITA AVE.                SE DECISION MADE: 21-JUL-03
SUNNYVALE, CA 94085               510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: MONOPLUS POLY-P-DIOXANONE MONOFILAMENT ABSORBABLE SURGICAL SUTUR
AESCULAP                          510(k) NO: K031216(TRADITIONAL)
ATTN: GEORG  KELLER               PHONE NO : 800-258-1946
3773 CORPORATE PKWY.              SE DECISION MADE: 17-JUL-03
CENTER VALLEY, PA 18034           510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: MODIFICATION TO MACS MODULAR ANTERIOR CONSTRUCT SYSTEM
AESCULAP, INC.                    510(k) NO: K032059(SPECIAL)
ATTN: GEORG  KELLER               PHONE NO : 610-797-9300
3773 CORPORATE PKWY.              SE DECISION MADE: 25-JUL-03
CENTER VALLEY, PA 18034           510(k) SUMMARY AVAILABLE FROM FDA

 
DEVICE: SIGNATURE EDITION INFUSION PUMP, SIGNATURE EDITION ADMINISTRATIO
ALARIS MEDICAL SYSTEMS, INC.      510(k) NO: K032147(SPECIAL)
ATTN: STACY L LEWIS               PHONE NO : 858-458-7830
10221 WATERIDGE CIR.              SE DECISION MADE: 25-JUL-03
SAN DIEGO, CA 92121               510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: SOFT (HYDROPHILIC) CONTACT LENS CARE SOLUTION
ALCON, INC.                       510(k) NO: K031193(TRADITIONAL)
ATTN: KIM B KRACKE                PHONE NO : 817-551-8338
6201 SOUTH FREEWAY                SE DECISION MADE: 03-JUL-03
FORT WORTH, TX 76134-2099         510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: MODIFICATION TO REPROCESSED SYNTHES EXTERNAL FIXATION DEVICES
ALLIANCE MEDICAL CORP.            510(k) NO: K032058(SPECIAL)
ATTN: MOIRA  BARTON               PHONE NO : 480-763-5300
10232 SOUTH 51ST ST.              SE DECISION MADE: 30-JUL-03
PHOENIX, AZ 85044                 510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: AMERICAN SYRINGE COMPANY 1CC AND 3CC SYRINGE
AMERICAN SYRINGE COMPANY          510(k) NO: K031394(TRADITIONAL)
ATTN: DAVID M GARVIN              PHONE NO : 305-371-8166
1200 BRICKELL AVE.                SE DECISION MADE: 25-JUL-03
SUITE 1480                        510(k) STATEMENT
MIAMI, FL 33131

DEVICE: AMERITEK SURE-POINT HDR NEEDLE TEMPLATE
AMERTEK MEDICAL, INC.             510(k) NO: K031273(TRADITIONAL)
ATTN: GREG  WIITA                 PHONE NO : 561-842-7595
2655 NORTH OCEAN DR.              SE DECISION MADE: 15-JUL-03
SINGER ISLAND, FL 33404           510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: AMPLAID A756 SCREENING ADMITTANCE METER
AMPLAID                           510(k) NO: K031978(SPECIAL)
ATTN: DANIEL  KAMM                PHONE NO : 847-374-1727
PO BOX 7007                       SE DECISION MADE: 21-JUL-03
DEERFIELD, IL 60015               510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: POWER LASER 90
ANDI ELECTROMEDICAL APS           510(k) NO: K030692(TRADITIONAL)
ATTN: JEFF  WORRELL               PHONE NO : 800-662-7283
12415 OLD MERIDIAN ST.            SE DECISION MADE: 17-JUL-03
CARMEL, IN 46032                  510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: A/C ENZYMATIC HOMOCYSTEINE ASSAY
ANTICANCER INC                    510(k) NO: K030754(TRADITIONAL)
ATTN: YUYING  TAN                 PHONE NO : 858-654-2555
7917 OSTROW ST.                   SE DECISION MADE: 11-JUL-03
SAN DIEGO, CA 92111               510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: INJECTOR
ANTON MEYER & CO. LTD.            510(k) NO: K023737(TRADITIONAL)
ATTN: THOMAS  MEYER               PHONE NO : 41 32 3329111
HELMSTRASSE 1                     SE DECISION MADE: 14-JUL-03
NIDAU, SWITZERLAND CH-2560        510(k) SUMMARY AVAILABLE FROM FDA

 
DEVICE: VINYL EXAMINATION GLOVES, POWDER FREE, VIOLET COLOR
ARISTA LATINDO INDUSTRIAL, LTD. P.510(k) NO: K031913(TRADITIONAL)
ATTN: LINGA  SUMARTA              PHONE NO : 621 166 20201/195
128 JALAN KYAI HAJI MUHAMMAD      SE DECISION MADE: 09-JUL-03
MANSYUR                           510(k) STATEMENT
JAKARTA BARAT, INDONESIA 11210

DEVICE: SPECIAL+, S-NEEDLE J-TYPE, S-NEEDLE B-TYPE
ASIA-MED GMBH AND CO KG           510(k) NO: K031716(TRADITIONAL)
ATTN: KEVIN  WALLS                PHONE NO : 720-962-5412
13 RED FOX LN.                    SE DECISION MADE: 10-JUL-03
LITTLETON, CO 80127               510(k) STATEMENT

DEVICE: OSTEO-G BONE VOID FILLER SYSTEM
ASPINE USA, INC.                  510(k) NO: K031319(TRADITIONAL)
ATTN: FLOYD G LARSON              PHONE NO : 858-792-1235
4329 GRAYDON RD.                  SE DECISION MADE: 17-JUL-03
SAN DIEGO, CA 92130               510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: AURORA
AURORA IMAGING TECHNOLOGY, INC.   510(k) NO: K032082(SPECIAL)
ATTN: JAMES R VEALE               PHONE NO : 719-495-3438
49 PLAIN STREET                   SE DECISION MADE: 30-JUL-03
NORTH ATTLEBORO, MA 02760         510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: DURAMAX .035 BILIARY STENT SYSTEM, MODELS DML0718-80, DML0718-13
AVANTEC VASCULAR CORP.            510(k) NO: K030638(TRADITIONAL)
ATTN: JAMES M SHY                 PHONE NO : 408-743-3100
1049 KIEL CT.                     SE DECISION MADE: 09-JUL-03
SUNNYVALE, CA 94089               510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: SAFETY INTRODUCER NEEDLE
B. BRAUN MEDICAL, INC.            510(k) NO: K030135(TRADITIONAL)
ATTN: AMY K SMITH                 PHONE NO : 610-266-0500
901 MARCON BLVD.                  SE DECISION MADE: 15-JUL-03
ALLENTOWN, PA 18109               510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: B. BRAUN NERVE BLOCK CATHETER
B. BRAUN MEDICAL, INC.            510(k) NO: K030830(TRADITIONAL)
ATTN: PATRICIA D WILSON           PHONE NO : 610-266-0500
901 MARCON BLVD.                  SE DECISION MADE: 15-JUL-03
ALLENTOWN, PA 18109               510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: BAYLIS PAIN MANAGEMENT GENERATOR, MODELS PMG-115-TD AND PMG-230-
BAYLIS MEDICAL CO., INC.          510(k) NO: K031950(ABBREVIATED)
ATTN: KRIS  SHAH                  PHONE NO : 905 602 4875
5160 EXPLORER DR. #33             SE DECISION MADE: 17-JUL-03
MISSISSAUGA, ONTARIO, CANADA L4W 4510(k) STATEMENT

DEVICE: SYNCHRON SYSTEMS VALPROIC ACID (V-PA) REAGENT
BECKMAN COULTER, INC.             510(k) NO: K031870(SPECIAL)
ATTN: MARY BETH  TANG             PHONE NO : 714-961-3777
200 SOUTH KRAEMER BLVD.           SE DECISION MADE: 15-JUL-03
BREA, CA 92822                    510(k) SUMMARY AVAILABLE FROM FDA

 
DEVICE: COULTER ACT 5DIFF AL HEMATOLOGY ANALYZER
BECKMAN COULTER, INC.             510(k) NO: K032013(SPECIAL)
ATTN: LOURDES  COBA               PHONE NO : 305-380-4552
11800 SW 147TH AVE.               SE DECISION MADE: 24-JUL-03
MIAMI, FL 33196-2500              510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: BD PHOENIX AUTOMATED MICROBIOLOGY SYSTEM-NITROFURANTOIN-8-512 UG
BECTON DICKINSON & CO.            510(k) NO: K031530(TRADITIONAL)
ATTN: MONICA EVELYN  GIGUERE      PHONE NO : 410-316-4287
7 LOVETON CIR.                    SE DECISION MADE: 10-JUL-03
SPARKS, MD 21152                  510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: BD PHOENIX AUTOMATED MICROBIOLOGY SYSTEM-NITROFURANTOIN GRAM POS
BECTON, DICKINSON AND COMPANY     510(k) NO: K031589(TRADITIONAL)
ATTN: MICHELLE B BANDY            PHONE NO : 410-316-4778
7 LOVETON CIR.                    SE DECISION MADE: 11-JUL-03
SPARKS, MD 21152-0999             510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: BD PHONENIX AUTOMATED MICROBIOLOGY SYSTEM
BECTON, DICKINSON AND COMPANY     510(k) NO: K031679(TRADITIONAL)
ATTN: BRADFORD  SPRING            PHONE NO : 410-316-4206
7 LOVETON CIR.                    SE DECISION MADE: 16-JUL-03
SPARKS, MD 21152-0999             510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: BD PHOENIX AUTOMATED MICROBIOLOGY SYSTEM - TRIMETHOPRIM-SULFAMET
BECTON, DICKINSON AND COMPANY     510(k) NO: K031699(TRADITIONAL)
ATTN: KATHRYN  BABKA POWERS       PHONE NO : 410-316-4260
7 LOVETON CIR.                    SE DECISION MADE: 30-JUL-03
SPARKS, MD 21152-0999             510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: BD PHOENIX AUTOMATED MICRBIOLOGY SYSTEM AMOXICILLIN/CLAVUALANTE
BECTON, DICKINSON AND COMPANY     510(k) NO: K031912(TRADITIONAL)
ATTN: MICHELLE B BANDY            PHONE NO : 410-316-4778
7 LOVETON CIR.                    SE DECISION MADE: 21-JUL-03
SPARKS, MD 21152-0999             510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: MICROHEATER
BELMONT INSTRUMENT CORP.          510(k) NO: K031478(TRADITIONAL)
ATTN: URAIWAN P LABADINI          PHONE NO : 978-663-0212
780 BOSTON RD.                    SE DECISION MADE: 02-JUL-03
BILLERICA, MA 01821               510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: BIO-LOGIC INSERT EARPHONES
BIO-LOGIC SYSTEMS CORP.           510(k) NO: K031352(TRADITIONAL)
ATTN: ERIK C GUNDERSEN            PHONE NO : 847-949-5200
ONE BIO-LOGIC PLAZA               SE DECISION MADE: 16-JUL-03
MUNDELEIN, IL 60060-3700          510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: PROFESSIONAL BLOOD SAMPLE RETRIEVAL SYSTEM
BIOMED PERSONAL METABOLIC AND NUTR510(k) NO: K030076(TRADITIONAL)
ATTN: SUSAN B FENTRESS            PHONE NO : 901-680-7319
6075 POPLAR AVE.                  SE DECISION MADE: 07-JUL-03
SUITE 500                         510(k) STATEMENT
MEMPHIS, TN 38119

 
DEVICE: VITEK 2 GRAM POSITIVE LINEZOLID FOR STREPTOCOCCUS PNEUMONIAE
BIOMERIEUX, INC.                  510(k) NO: K031410(TRADITIONAL)
ATTN: NANCY  WEAVER               PHONE NO : 314-731-8695
595 ANGLUM RD.                    SE DECISION MADE: 10-JUL-03
HAZELWOOD, MO 63042-2320          510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: BACT/ALERT MP CULTURE BOTTLES (PLASTIC)
BIOMERIEUX, INC.                  510(k) NO: K031737(TRADITIONAL)
ATTN: JOCELYN  JENNINGS           PHONE NO : 919-620-2968
100 RODOLPHE ST.                  SE DECISION MADE: 14-JUL-03
DURHAM, NC 27712                  510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: GENERATION 4 POLISHED FEMORAL HIP PROSTHESIS
BIOMET, INC.                      510(k) NO: K031734(SPECIAL)
ATTN: GARY  BAKER                 PHONE NO : 574-372-1568
56 EAST BELL DR.                  SE DECISION MADE: 01-JUL-03
PO BOX 587                        510(k) SUMMARY AVAILABLE FROM FDA
WARSAW, IN 46581-0587

DEVICE: AIRBRUSH LIPOSCULPTOR SYSTEM
BIOSCULPTURE TECHNOLOGY, INC.     510(k) NO: K031881(TRADITIONAL)
ATTN: ROBERT  CUCIN               PHONE NO : 212-977-5400
120 CENTRAL PARK SOUTH            SE DECISION MADE: 28-JUL-03
NEW YORK, NY 10019                510(k) SUMMARY AVAILABLE FROM FDA
                                  THIRD PARTY REVIEW

DEVICE: VARIABLE LASSO 2515 CIRCULAR MAPPING CATHETER
BIOSENSE WEBSTER, INC.            510(k) NO: K031161(SPECIAL)
ATTN: WILLIAM  WELCH              PHONE NO : 909-839-8604
3333 DIAMOND CANYON RD.           SE DECISION MADE: 22-JUL-03
DIAMOND BAR, CA 91765             510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: GENERAL SEMEN ANALYSIS (GSA) KIT
BIOSHAF LTD.                      510(k) NO: K024337(TRADITIONAL)
ATTN: TOM  TSAKERIS               PHONE NO : 301-330-2076
16809 BRIARDALE RD.               SE DECISION MADE: 03-JUL-03
ROCKVILLE, MD 20855               510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: INTRAOS 70
BLUE X IMAGING SRL                510(k) NO: K031118(TRADITIONAL)
ATTN: AL  SOSA                    PHONE NO : 847-459-3889
251 E. DUNDEE RD.                 SE DECISION MADE: 08-JUL-03
SUITE #6                          510(k) SUMMARY AVAILABLE FROM FDA
WHEELING, IL 60090

DEVICE: ULTRAFLEX PRECISION COLONIC STENT
BOSTON SCIENTIFIC CORP.           510(k) NO: K030769(TRADITIONAL)
ATTN: KATHLEEN  MORAHAN           PHONE NO : 508-652-5942
ONE BOSTON SCIENTIFIC PLACE       SE DECISION MADE: 14-JUL-03
NATICK, MA 01760-1537             510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: VAXCEL WITH PASV PORT (LOW PROFILE), MODELS 45-236 AND 45-238
BOSTON SCIENTIFIC CORP.           510(k) NO: K031844(SPECIAL)
ATTN: JODI LYNN  GREENIZEN        PHONE NO : 518-742-4338
10 GLENS FALLS TECHNICAL PARK     SE DECISION MADE: 15-JUL-03
GLENS FALLS, NY 12801-3864        510(k) SUMMARY AVAILABLE FROM FDA

 
DEVICE: VAXCEL WITH PASV PORT, MODEL 45-213
BOSTON SCIENTIFIC CORP.           510(k) NO: K032008(SPECIAL)
ATTN: JODI LYNN  GREENIZEN        PHONE NO : 518-742-4338
ONE BOSTON SCIENTIFIC PL.         SE DECISION MADE: 14-JUL-03
NATICK, MA 01760-1537             510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: MONITECT OXYCODONE DRUG DCREEN CASSETTE TEST, MODEL MC 23, FASTE
BRANAN MEDICAL CORP.              510(k) NO: K030113(TRADITIONAL)
ATTN: RAPHAEL  WONG               PHONE NO : 949-598-7166
10015 MUIRLANDS RD., SUITE E      SE DECISION MADE: 02-JUL-03
IRVINE, CA 92618                  510(k) STATEMENT

DEVICE: BRODA MODEL 587 MANUAL WHEELCHAIR
BRODA ENT., INC.                  510(k) NO: K032133(TRADITIONAL)
ATTN: PHILLIP  MCTAGGART          PHONE NO : 541 746 8080
385 PHILLIP ST.                   SE DECISION MADE: 21-JUL-03
WATERLOO ONTARIO, CANADA N2L 5R8  510(k) SUMMARY AVAILABLE FROM FDA
                                  THIRD PARTY REVIEW

DEVICE: NIAGARA TEMPORARY DUAL LUMEN CATHETERS; FLEXXICON II TEMPORARY D
C.R. BARD, INC.                   510(k) NO: K030268(ABBREVIATED)
ATTN: GLENN  NORTON               PHONE NO : 801-595-0700
5425 WEST AMELIA EARHART DR.      SE DECISION MADE: 30-JUL-03
SALT LAKE CITY, UT 84116          510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: CATHETER REPAIR KIT WITH REPLACEMENT CONNECTOR, MODEL 5587000
C.R. BARD, INC.                   510(k) NO: K030442(TRADITIONAL)
ATTN: RAMON  RICART               PHONE NO : 801-595-0700
5425 WEST AMELIA EARHART DR.      SE DECISION MADE: 21-JUL-03
SALT LAKE CITY, UT 84116          510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: RECOVERY FILTER SYSTEM, MODEL RF-048F
C.R. BARD, INC.                   510(k) NO: K031328(ABBREVIATED)
ATTN: MARY J EDWARDS              PHONE NO : 480-303-2640
1625 WEST 3RD ST.                 SE DECISION MADE: 25-JUL-03
TEMPE, AZ 85280                   510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: X-PROT DUO PORT
C.R. BARD, INC.                   510(k) NO: K032044(SPECIAL)
ATTN: JOHN C KNORPP               PHONE NO : 801-595-0700
5425 WEST AMELIA EARHART DR.      SE DECISION MADE: 10-JUL-03
SALT LAKE CITY, UT 84116          510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: POWERHEART AED G3, MODEL 9300
CARDIAC SCIENCE                   510(k) NO: K031987(SPECIAL)
ATTN: KENNETH  OLSON              PHONE NO : 952-939-2912
5474 FELTL RD.                    SE DECISION MADE: 30-JUL-03
MINNEAPOLIS, MN 55343             510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: SAFETY RELEASE ARCH BAR KIT
CASEY SURGICAL, LLC               510(k) NO: K031207(TRADITIONAL)
ATTN: JAMES E STANLEY             PHONE NO : 816-347-9224
200 NE MULBERRY                   SE DECISION MADE: 15-JUL-03
SUITE 200                         510(k) SUMMARY AVAILABLE FROM FDA
LEE'S SUMMIT, MO 64086

 
DEVICE: CEFAR REHAB 2 AND REHAB 2 PRO
CEFAR MEDICAL AB                  510(k) NO: K030403(TRADITIONAL)
ATTN: CONSTANCE G BUNDY           PHONE NO : 763-571-1976
6740 RIVERVIEW TERRACE            SE DECISION MADE: 17-JUL-03
MINNEAPOLIS, MN 55432             510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: TIBIAL SPACER FOR THE NATURAL-KNEE II CEMENTED MODULAR TIBIAL BA
CENTERPULSE ORTHOPEDICS, INC.     510(k) NO: K031183(TRADITIONAL)
ATTN: ROBERT M WOLFARTH           PHONE NO : 512-432-9324
9900 SPECTRUM DR.                 SE DECISION MADE: 14-JUL-03
AUSTIN, TX 78717                  510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: CLEARMEDICAL/CRITIKON BLOOD PRESSURE CUFF; CLEARMEDICAL/WELCH AL
CLEAR MEDICAL, INC.               510(k) NO: K031416(TRADITIONAL)
ATTN: LANE  ABENROTH              PHONE NO : 425-401-1414
1776 136TH PL.  NE                SE DECISION MADE: 15-JUL-03
BELLEVUE, WA 98005                510(k) SUMMARY AVAILABLE FROM FDA
                                  THIRD PARTY REVIEW

DEVICE: ATAC PAK URIC ACID REAGENT AND ATAC CALIBRATOR
CLINICAL DATA, INC.               510(k) NO: K031044(TRADITIONAL)
ATTN: WYNN  STOCKING              PHONE NO : 714-672-3553
1075 W. LAMBERT ROAD              SE DECISION MADE: 15-JUL-03
BUILDING D                        510(k) SUMMARY AVAILABLE FROM FDA
BREA, CA 92821

DEVICE: BRAIN COIL, MODEL 9900GE-64
CLINICAL MR SOLUTIONS, LLC        510(k) NO: K031536(TRADITIONAL)
ATTN: RALPH S HASHOIAN            PHONE NO : 262-781-9394
3735 SHADYBROOK PLACE             SE DECISION MADE: 18-JUL-03
BROOKFIELD, WI 53005              510(k) STATEMENT

DEVICE: LINICAL PROTEIN 2 CALIBRATION VERIFIERS LEVELS A-E FOR OLYMPUS A
CLINIQA CORPORATION               510(k) NO: K031575(TRADITIONAL)
ATTN: CAROL  RUGGIERO             PHONE NO : 760-744-1900
1432 SOUTH MISSION RD.            SE DECISION MADE: 23-JUL-03
FALLBROOK, CA 92028               510(k) STATEMENT

DEVICE: MODIFICATION TO COALESCENT SURGICAL U-CLIP AND ACCESSORIES
COALESCENT SURGICAL               510(k) NO: K031623(SPECIAL)
ATTN: MICHAEL A DANIEL            PHONE NO : 415-407-0223
559 EAST WEDDELL DR.              SE DECISION MADE: 03-JUL-03
SUNNYVALE, CA 94089               510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: MODIFICATION TO HERMES O.R. CONTROL CENTER
COMPUTER MOTION, INC.             510(k) NO: K031720(SPECIAL)
ATTN: KEITH  LOWREY               PHONE NO : 805-685-3729
130 CREMONA DRIVE, SUITE B        SE DECISION MADE: 11-JUL-03
GOLETA, CA 93117                  510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: MODIFICATION TO HERMES O.R. CONTROL CENTER
COMPUTER MOTION, INC.             510(k) NO: K031956(SPECIAL)
ATTN: KEITH  LOWREY               PHONE NO : 805-685-3729
130-B CREMONA DR.                 SE DECISION MADE: 17-JUL-03
GOLETA, CA 93117                  510(k) SUMMARY AVAILABLE FROM FDA

 
DEVICE: CONMED INTEGRATED SYSTEMS NURSES ASSISTANT
CONMED INTEGRATED SYSTEMS (CMIS)  510(k) NO: K031979(SPECIAL)
ATTN: C. JEFF  LIPPS              PHONE NO : 503-614-1106
1815 NW 169TH PLACE               SE DECISION MADE: 25-JUL-03
SUITE 4020                        510(k) SUMMARY AVAILABLE FROM FDA
BEAVERTON, OR 97006

DEVICE: FILMLESS CLINIC
CONNECT IMAGING, INC.             510(k) NO: K031704(ABBREVIATED)
ATTN: PHILIP J MANLY              PHONE NO : 808-373-7048
850 WEST HIND DRIVE # 214         SE DECISION MADE: 31-JUL-03
HONOLULU, HI 96821                510(k) STATEMENT

DEVICE: COOK GASTRIC SIZING BALLOON CATHETER
COOK, INC.                        510(k) NO: K030841(TRADITIONAL)
ATTN: CAROL  ZWISSLER             PHONE NO : 812-339-2235
750 DANIELS WAY                   SE DECISION MADE: 11-JUL-03
P.O. BOX 489                      510(k) SUMMARY AVAILABLE FROM FDA
BLOOMINGTON, IN 47402-0489

DEVICE: MODIFICATION TO COOK ZILVER BILIARY STENT
COOK, INC.                        510(k) NO: K031821(SPECIAL)
ATTN: CAROL  ZWISSLER             PHONE NO : 812-339-2235
750 DANIELS WAY                   SE DECISION MADE: 18-JUL-03
P.O. BOX 489                      510(k) SUMMARY AVAILABLE FROM FDA
BLOOMINGTON, IN 47402-0489

DEVICE: CORIX 70 PLUS-USV
CORAMEX, S.A.                     510(k) NO: K031802(TRADITIONAL)
ATTN: AL  SOSA                    PHONE NO : 847-459-3889
251 E. DUNDEE ROAD SUITE #6       SE DECISION MADE: 21-JUL-03
WHEELING, IL 60090                510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: MODEIFICATION TO: SMART CONTROL NITINOL STENT TRANSHEPATIC BILIA
CORDIS CORP.                      510(k) NO: K031777(SPECIAL)
ATTN: SAM  MIRZA                  PHONE NO : 786-313-2007
14201 N.W. 60TH AVE.              SE DECISION MADE: 07-JUL-03
MIAMI LAKES, FL 33014             510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: REAADS IGM ANTI-B2GPI TEST KIT, MODEL 038-001
CORGENIX, INC.                    510(k) NO: K031208(SPECIAL)
ATTN: NANCI  DEXTER               PHONE NO : 303-457-4345
12061 TEJON ST.                   SE DECISION MADE: 07-JUL-03
WESTMINSTER, CO 80234             510(k) STATEMENT

DEVICE: CRYOSTAR SYSTEM, COMPRISING: A) CRYOSTAR CONSOLE, B) CRYOSTAR 1M
CRYOMEDICAL INSTRUEMTS LTD.       510(k) NO: K031482(TRADITIONAL)
ATTN: GARETH  COPPING             PHONE NO : 44 162 3424200
CRYOMED HOUSE, GROVE WAY          SE DECISION MADE: 10-JUL-03
MANSFIELD WOODHOUSE, NOTTS, UNITED510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: CYNOSURE PHOTOLIGHT PL
CYNOSURE, INC.                    510(k) NO: K031258(TRADITIONAL)
ATTN: GEORGE  CHO                 PHONE NO : 978-256-4200
10 ELIZABETH DR.                  SE DECISION MADE: 08-JUL-03
CHELMSFORD, MA 01824              510(k) SUMMARY AVAILABLE FROM FDA

 
DEVICE: CYNOSURE YAG FAMILY LASER (PHOTOGENICA YAG AND ACCLAIM)
CYNOSURE, INC.                    510(k) NO: K031690(TRADITIONAL)
ATTN: GEORGE  CHO                 PHONE NO : 978-256-4200
10 ELIZABETH DR.                  SE DECISION MADE: 08-JUL-03
CHELMSFORD, MA 01824              510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: EMIT II PLUS COCAINE METABOLITE ASSAY
DADE BEHRING, INC.                510(k) NO: K031512(TRADITIONAL)
ATTN: KATHLEEN A DRAY-LYONS       PHONE NO : 781-826-4551
P.O. BOX 6101                     SE DECISION MADE: 23-JUL-03
NEWARK,, DE 19714                 510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: MICROSCAN RAPID/S PLUS GRAM-NEGATIVE MIC/COMBO PANEL WITH NITROF
DADE BEHRING, INC.                510(k) NO: K031602(TRADITIONAL)
ATTN: ROBERT  EUSEBIO             PHONE NO : 916-374-3183
2040 ENTERPRISE BLVD.             SE DECISION MADE: 31-JUL-03
WEST SACRAMENTO, CA 95691         510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: STAINLESS STEEL AQUATIC WHEELCHAIR
DB PERKS & ASSOCIATES LTD.        510(k) NO: K031910(TRADITIONAL)
ATTN: ED  OLIVER                  PHONE NO : 425-557-9990
490 NW DATEWOOD DRIVE             SE DECISION MADE: 25-JUL-03
ISSAQUAH, WA 98027                510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: SLED CURING LIGHT SYSTEM
DENTSPLY INTERNATIONAL            510(k) NO: K031615(TRADITIONAL)
ATTN: P. JEFFERY  LEHN            PHONE NO : 717-845-7511
570 WEST COLLEGE AVE.             SE DECISION MADE: 21-JUL-03
YORK, PA 17405-0872               510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: ESTYLUS ELECTRIC MOTOR SYSTEM
DENTSPLY INTL.                    510(k) NO: K031145(TRADITIONAL)
ATTN: P. JEFFERY  LEHN            PHONE NO : 717-845-7511
570 WEST COLLEGE AVE.             SE DECISION MADE: 15-JUL-03
YORK, PA 17404                    510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: BIAX A.F. WRIST/BIAX ADVANCED FIXATION WRIST
DEPUY ORTHOPAEDICS, INC.          510(k) NO: K031203(TRADITIONAL)
ATTN: DINA L WEISSMAN             PHONE NO : 574-371-4905
700 ORTHOPAEDIC DR.               SE DECISION MADE: 14-JUL-03
P.O. BOX 988                      510(k) SUMMARY AVAILABLE FROM FDA
WARSAW, IN 46581-0988

DEVICE: DEPUY CERAMIC FEMORAL HEADS
DEPUY ORTHOPAEDICS, INC.          510(k) NO: K031803(SPECIAL)
ATTN: KARLA A HAM                 PHONE NO : 574-371-4925
700 ORTHOPAEDIC DR.               SE DECISION MADE: 01-JUL-03
P.O. BOX 988                      510(k) SUMMARY AVAILABLE FROM FDA
WARSAW, IN 46581-0988

DEVICE: DEPUY RESTORE ORTHOBIOLOGIC SOFT TISSUE IMPLANT
DEPUY ORTHOPAEDICS, INC.          510(k) NO: K031969(TRADITIONAL)
ATTN: KATHY K TRIER               PHONE NO : 574-372-5039
700 ORTHOPAEDIC DR.               SE DECISION MADE: 28-JUL-03
P.O. BOX 988                      510(k) SUMMARY AVAILABLE FROM FDA
WARSAW, IN 46581-0988

 
DEVICE: DIADEXUS PLAC TEST
DIADEXUS, INC.                    510(k) NO: K030477(TRADITIONAL)
ATTN: ROBERT L WOLFERT            PHONE NO : 650-246-6400
343 OYSTER POINT BLVD.            SE DECISION MADE: 18-JUL-03
SOUTH SAN FRANCISCO, CA 94080     510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: IDEAL MIMESYS SYSTEM WITH INTEGRATED VENOUS AIR REMOVAL, CENTRIF
DIDECO S.P.A.                     510(k) NO: K032040(SPECIAL)
ATTN: BARRY  SALL                 PHONE NO : 781-434-4742
195 WEST ST.                      SE DECISION MADE: 09-JUL-03
WALTHAM, MA 02451-1163            510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: FABIUS TIRO ANESTHESIA SYSTEM
DRAEGER MEDICAL, INC.             510(k) NO: K031400(SPECIAL)
ATTN: MICHAEL A KELHART           PHONE NO : 215-721-5400
3135 QUARRY RD.                   SE DECISION MADE: 15-JUL-03
TELFORD, PA 18969                 510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: SITE-RITE IV ULTRASOUND SYSTEM
DYMAX CORP.                       510(k) NO: K032135(TRADITIONAL)
ATTN: CHARLES  MORREALE           PHONE NO : 412-963-6884
271 KAPPA DR.                     SE DECISION MADE: 21-JUL-03
PITTSBURGH, PA 15238              510(k) SUMMARY AVAILABLE FROM FDA
                                  THIRD PARTY REVIEW

DEVICE: EARLYDETECT MENOPAUSE TEST FOR FSH
EARLY DETECT, INC.                510(k) NO: K030058(TRADITIONAL)
ATTN: PETER  GEORGE               PHONE NO : 714-283-5190
2950 NORTH GLASSELL ST.           SE DECISION MADE: 30-JUL-03
ORANGE, CA 92865                  510(k) STATEMENT

DEVICE: EBI XFIX OPTIROM KNEE FIXATOR
EBI, L.P.                         510(k) NO: K031093(TRADITIONAL)
ATTN: JON  CAPAROTTA              PHONE NO : 973-299-9300
100 INTERPACE PKWY.               SE DECISION MADE: 10-JUL-03
PARSIPPANY, NJ 07054              510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: EBI SPINELINK - II SPINAL FIXATION SYSTEM
EBI, L.P.                         510(k) NO: K031355(TRADITIONAL)
ATTN: FREDERIC  TESTA             PHONE NO : 973-299-9300
100 INTERPACE PKWY.               SE DECISION MADE: 22-JUL-03
PARSIPPANY, NJ 07054              510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: EBI SPINELINK SPINAL FIXATION SYSTEM
EBI, L.P.                         510(k) NO: K031424(TRADITIONAL)
ATTN: BARRY  SANDS                PHONE NO : 973-299-9300
100 INTERPACE PKWY.               SE DECISION MADE: 22-JUL-03
PARSIPPANY, NJ 07054              510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: AEROLET TOILET LIFT, MODEL AER-01
ECONOMIC HOLLAND B.V.             510(k) NO: K031045(TRADITIONAL)
ATTN: STEPHANIE  WOLFKAMP         PHONE NO : 336-766-7686
6785 FOREST OAK DR.               SE DECISION MADE: 10-JUL-03
CLEMMONS, NC 27012                510(k) SUMMARY AVAILABLE FROM FDA

 
DEVICE: EDWARDS LIFESCIENCES LIFESTENT NT18 SELF-EXPANDING BILIARY STENT
EDWARDS LIFESCIENCES, LLC.        510(k) NO: K024303(TRADITIONAL)
ATTN: KAVIN  DRISKO               PHONE NO : 949-250-2416
ONE EDWARDS WAY                   SE DECISION MADE: 03-JUL-03
IRVINE, CA 92614                  510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: EKOS PERIPHERAL INFUSION SYSTEM
EKOS CORP.                        510(k) NO: K030637(TRADITIONAL)
ATTN: JOCELYN  KERSTEN            PHONE NO : 425-482-1108
22030 20TH AVENUE S.E.            SE DECISION MADE: 22-JUL-03
SUITE 101                         510(k) SUMMARY AVAILABLE FROM FDA
BOTHELL, WA 98021

DEVICE: CARDIO VASCULAR INFORMATION ENHANCED WORKSTATION
ELECTROMED IMAGING INC.           510(k) NO: K031638(ABBREVIATED)
ATTN: WARREN  BAKER               PHONE NO : 450 681 3925
440 ARMAND-FRAPPIER BLVD.,#250    SE DECISION MADE: 21-JUL-03
LAVAL, QUEBEC, CANADA H7V 4B4     510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: ELECTROMEDICARIN 900
ELECTROMEDICARIN, S.A.            510(k) NO: K020478(ABBREVIATED)
ATTN: JAY  MANSOUR                PHONE NO : 678-908-8180
1308 MORNINGSIDE PARK DR.         SE DECISION MADE: 17-JUL-03
ALPHARETTA, GA 30022              510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: MODIFICATION TO LEKSELL STEREOTACTIC SYSTEM
ELEKTA INSTRUMENT AB              510(k) NO: K031980(SPECIAL)
ATTN: PETER  LOWENDAHL            PHONE NO : 46 8 58725400
BIRGER JARLSGATAN 53              SE DECISION MADE: 25-JUL-03
PO BOX 7593                       510(k) STATEMENT
STOCKHOLM, SWEDEN SE-103 93

DEVICE: ELEKTA LEKSELL STEREOTACTIC SYSTEM WITH MR POST KIT
ELEKTA INSTRUMENT AB              510(k) NO: K031999(SPECIAL)
ATTN: PETER  LOWENDAHL            PHONE NO : 46 8 58725400
BIRGER JARLSGATAN 53              SE DECISION MADE: 25-JUL-03
STOCKHOLM, SWEDEN S-103 93        510(k) STATEMENT

DEVICE: CARDIOVATIONS OPTICAL BIPOLAR DEVICE
ETHICON, INC.                     510(k) NO: K031846(SPECIAL)
ATTN: PETER  CECCHINI             PHONE NO : 908-218-2457
ROUTE 22 WEST                     SE DECISION MADE: 21-JUL-03
SOMERVILLE, NJ 08876              510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: CARDIOVATIONS RETRACTOR
ETHICON, INC.                     510(k) NO: K031847(SPECIAL)
ATTN: PETER  CECCHINI             PHONE NO : 908-218-2457
ROUTE 22 WEST                     SE DECISION MADE: 21-JUL-03
SOMERVILLE, NJ 08876              510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: LORDEX POWER TRACTION EQUIPMENT
EVER PROSPEROUS INSTRUMENT INC    510(k) NO: K031227(TRADITIONAL)
ATTN: JOHN  BOREN                 PHONE NO : 281-398-1700
15915 KATY FREEWAY                SE DECISION MADE: 17-JUL-03
SUITE 645                         510(k) STATEMENT
HOUSTON, TX 77094

 
DEVICE: EXCEL PRIMARY SOLUTION SET
EXELINT INTL. CO.                 510(k) NO: K031500(TRADITIONAL)
ATTN: ARMAND  HAMID               PHONE NO : 310-649-0707
5840 WEST CENTINELA AVE.          SE DECISION MADE: 25-JUL-03
LOS ANGELES, CA 90045             510(k) STATEMENT

DEVICE: FEMTEX JUNIOR/SLENDER REGULAR OPEN-END TAMPONS
FIRST QUALITY HYGIENIC, INC.      510(k) NO: K031067(TRADITIONAL)
ATTN: ROBERT J STAAB              PHONE NO : 201-327-0035
73 FRANKLIN TURNPIKE              SE DECISION MADE: 14-JUL-03
ALLENDALE, NJ 07401               510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: RESPIRATORY HUMIDIFIER, MODEL MR850
FISHER & PAYKEL HEALTHCARE, LTD.  510(k) NO: K020332(TRADITIONAL)
ATTN: BRETT  WHISTON              PHONE NO : 649 574 0100
15 MAURICE PAYKEL PLACE           SE DECISION MADE: 07-JUL-03
EAST TAMAKI, NEW ZEALAND          510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: NATURALASE LP ND:YAG LASER
FOCUS MEDICAL, LLC.               510(k) NO: K031828(TRADITIONAL)
ATTN: JOHN  LEE, JR               PHONE NO : 203-730-8885
23 FRANCIS J. CLARKE CIRCLE       SE DECISION MADE: 17-JUL-03
BETHEL, CT 06801                  510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: FOTONA FIDELIS PLUS ND:YAG LASER SYSTEM
FOTONA D.D.                       510(k) NO: K024204(TRADITIONAL)
ATTN: MOJCA  VALJAVEC             PHONE NO : 386 1 5009114
STEGNE 7,                         SE DECISION MADE: 07-JUL-03
LJUBLJANA, SLOVENIA 1210          510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: GALT MEDICAL GUIDEWIRE
GALT MEDICAL CORP.                510(k) NO: K031916(SPECIAL)
ATTN: DAVID  CATLIN               PHONE NO : 972-271-5177
2475 MERRITT DR.                  SE DECISION MADE: 17-JUL-03
GARLAND, TX 75041                 510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: DPX SERIES BRAVO DUO BONE DENSITOMETER
GE LUNAR CORP.                    510(k) NO: K030962(TRADITIONAL)
ATTN: JAMES P RASKOB              PHONE NO : 608-826-7425
726 HEARTLAND TRAIL               SE DECISION MADE: 25-JUL-03
MADISON, WI 53717                 510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: GE DELTA SOFTWARE OPTION FOR MRI
GE MEDICAL SYSTEMS                510(k) NO: K031927(TRADITIONAL)
ATTN: LARRY  KREGER               PHONE NO : 262-544-3464
3200 N. GRANDVIEW BLVD.           SE DECISION MADE: 02-JUL-03
WAUKESHA, WI 53188                510(k) SUMMARY AVAILABLE FROM FDA
                                  THIRD PARTY REVIEW

DEVICE: 8 CHANNEL CARDIAC PHASED ARRAY COIL
GE MEDICAL SYSTEMS                510(k) NO: K032045(SPECIAL)
ATTN: LARRY  KROGER               PHONE NO : 262-544-3894
P.O. BOX 414                      SE DECISION MADE: 30-JUL-03
MILWAUKEE, WI 53201               510(k) SUMMARY AVAILABLE FROM FDA

 
DEVICE: DINAMAP PRO 1000 V3 MONITOR, MODEL 1100 SERIES
GE MEDICAL SYSTEMS INFORMATION TEC510(k) NO: K031376(SPECIAL)
ATTN: MELISSA  ROBINSON           PHONE NO : 817-887-2133
4502 WOODLAND CORP.BLVD.          SE DECISION MADE: 16-JUL-03
TAMPA, FL 33614                   510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: GEBAUER'S SKIN REFRIGERANT (MIST SPRAY), MODEL P/N 0386-0010-07,
GEBAUER CO.                       510(k) NO: K031036(TRADITIONAL)
ATTN: AMY J PAUKOVITS             PHONE NO : 216-271-5252
9410 ST. CATHERINE AVE.           SE DECISION MADE: 10-JUL-03
CLEVELAND, OH 44104               510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: GE LOGIQ 7, MODEL 2354858
GENERAL ELECTRIC CO.              510(k) NO: K032182(SPECIAL)
ATTN: ALLEN  SCHUH                PHONE NO : 414-647-4385
P.O. BOX 414                      SE DECISION MADE: 25-JUL-03
MILWAUKEE, WI 53201               510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: S-1150 PLEUR-EVAC SAHARA PLUS CONTINUOUS REINFUSION AUTOTRANSFUS
GENZYME BIOSURGERY                510(k) NO: K031554(TRADITIONAL)
ATTN: DENISE  LIMA                PHONE NO : 508-677-6439
600 AIRPORT RD.                   SE DECISION MADE: 25-JUL-03
FALL RIVER, MA 02720-4740         510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: BIOSIGN SSI BIOLOGICAL TEST PACK WITH INSTANT READOUT INTEGRATOR
GETINGE USA, INC                  510(k) NO: K031647(TRADITIONAL)
ATTN: KARLA  BYRNE                PHONE NO : 585-272-5007
1777 EAST HENRIETTA RD.           SE DECISION MADE: 29-JUL-03
ROCHESTER, NY 14623-3133          510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: GIVEN DIAGNOSTIC SYSTEM
GIVEN IMAGING LTD.                510(k) NO: K031033(TRADITIONAL)
ATTN: SHOSHANA  FRIEDMAN          PHONE NO : 972 490 97784
NEW INDUSTRIAL PARK               SE DECISION MADE: 01-JUL-03
P.O. BOX 258                      510(k) SUMMARY AVAILABLE FROM FDA
YOQNEAM, ISRAEL 20692

DEVICE: NON-STERILE, POWDER-FREE, BLUE COLOR NITRILE EXAMINATION GLOVE
GREEN PROSPECT SDN BHD            510(k) NO: K031580(TRADITIONAL)
ATTN: JANNA P TUCKER              PHONE NO : 775-342-2612
198 AVENUE DE LA D'EMERALD        SE DECISION MADE: 25-JUL-03
SPARKS, NV 89434-9550             510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: NON-STERILE POWDER FREE, LATEX EXAMINATION GLOVES, POLYMER COATE
GREEN PROSPECT SDN BHD            510(k) NO: K031581(TRADITIONAL)
ATTN: JANNA P TUCKER              PHONE NO : 775-342-2612
198 AVENUE DE LA D'EMERALD        SE DECISION MADE: 24-JUL-03
SPARKS, NV 89434-9550             510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: MODIFICATION TO ZAP GUARD DEFIBRILLATOR TEST PROBE
GUARDIAN ANGEL PRODUCTS, INC.     510(k) NO: K030547(SPECIAL)
ATTN: ERNEST H PESCATORE          PHONE NO : 215-938-7677
2771 PHILMONT AVE.                SE DECISION MADE: 11-JUL-03
HUNTINGDON VALLEY, PA 19006       510(k) SUMMARY AVAILABLE FROM FDA

 
DEVICE: RAPIDO CUT-AWAY CUTTER
GUIDANT CORP.                     510(k) NO: K031459(TRADITIONAL)
ATTN: SHAH  HILALI                PHONE NO : 651-582-7752
4100 HAMLINE AVE., NORTH          SE DECISION MADE: 23-JUL-03
ST. PAUL, MN 55112-5798           510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: RAPIDO CUT-A-WAY ROTATING HEMOSTASIS VALVE
GUIDANT CORPORATION               510(k) NO: K031688(SPECIAL)
ATTN: STEPHANIE  ISGRIGG ROBINSON PHONE NO : 651-582-4927
4100 HAMLINE AVE NORTH            SE DECISION MADE: 02-JUL-03
ST PAUL, MN 55112-5798            510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: GYRUS PLASMAKINETIC SUPERPULSE SYSTEM (GENERATOR, ACCESSORIES)
GYRUS MEDICAL, INC.               510(k) NO: K031085(TRADITIONAL)
ATTN: MERCEDES  BAYANI            PHONE NO : 763-416-3015
6655 WEDGWOOD RD.                 SE DECISION MADE: 21-JUL-03
SUITE 105                         510(k) SUMMARY AVAILABLE FROM FDA
MAPLE GROVE, MN 55311-3602

DEVICE: HL168R
HEALTH & LIFE CO., LTD.           510(k) NO: K031695(SPECIAL)
ATTN: SUSAN  CHEN                 PHONE NO : 886 282 271300
9F, NO.186, JIAN YI ROAD          SE DECISION MADE: 01-JUL-03
CHUNG HO CITY, TAIPEI, HSIEN, CHIN510(k) STATEMENT

DEVICE: HL888RA
HEALTH & LIFE CO., LTD.           510(k) NO: K031835(SPECIAL)
ATTN: SUSAN  CHEN                 PHONE NO : 886 282 271300
9F, NO.186, JIAN YI ROAD          SE DECISION MADE: 01-JUL-03
CHUNG HO CITY, TAIPEI, HSIEN, CHIN510(k) STATEMENT

DEVICE: SUILE WOUND DRESSING
HEDONIST BIOCHEMICAL TECHNOLOGIES 510(k) NO: K022967(TRADITIONAL)
ATTN: ERIC  LUO                   PHONE NO : 972-491-2059
6833 SAINT LAWRENCE ST.           SE DECISION MADE: 08-JUL-03
PLANO, TX 75024                   510(k) STATEMENT

DEVICE: HOFFRICHTER VECTOR, VECTOR PLUS, VECTOR BI-VEVEL, VECTOR BI-LEVE
HOFFRICHTER GMBH                  510(k) NO: K014074(TRADITIONAL)
ATTN: STEPHEN H GORSKI            PHONE NO : 262-594-2114
S65 W35739 PIPER RD.              SE DECISION MADE: 23-JUL-03
EAGLE, WI 53119                   510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: TRUETRACK SMART SYSTEM BLOOD GLUCOSE METER AND TRUE TRACK SMART
HOME DIAGNOSTICS, INC.            510(k) NO: K030703(TRADITIONAL)
ATTN: KAREN  DEVINCENT            PHONE NO : 954-677-9201
2400 N.W. 55TH CT.                SE DECISION MADE: 11-JUL-03
FORT LAUDERDALE, FL 33309         510(k) STATEMENT

DEVICE: LIFEVALVE CENTRAL VENOUS CATHTER
HORIZON MEDICAL PRODUCTS, INC.    510(k) NO: K031718(SPECIAL)
ATTN: SCOTT  MOELLER              PHONE NO : 800-472-5221
1 HORIZON WAY                     SE DECISION MADE: 02-JUL-03
MANCHESTER, GA 31816              510(k) SUMMARY AVAILABLE FROM FDA

 
DEVICE: GLOBAL MODULAR REPLACEMENT SYSTEM PEDIATRIC TIBIAL BEARING COMPO
HOWMEDICA OSTEONICS CORP.         510(k) NO: K031480(TRADITIONAL)
ATTN: MARGARET F CROWE            PHONE NO : 201-831-5580
59 ROUTE 17 SOUTH                 SE DECISION MADE: 31-JUL-03
ALLENDALE, NJ 07401               510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: XIA SPINAL SYSTEM AND XIA STAINLESS STEEL SYSTEM
HOWMEDICA OSTEONICS CORP.         510(k) NO: K031893(SPECIAL)
ATTN: KAREN  ARIEMMA              PHONE NO : 201-831-5718
59 ROUTE 17                       SE DECISION MADE: 17-JUL-03
ALLENDALE, NJ 07401-1677          510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: HOFFMANN II COMPACT BALTIMORE COUPLING
HOWMEDICA OSTEONICS CORP.         510(k) NO: K031941(SPECIAL)
ATTN: VIVIAN  KELLY               PHONE NO : 201-831-5581
59 ROUTE 17                       SE DECISION MADE: 24-JUL-03
ALLENDALE, NJ 07401-1677          510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: STRYKER PLATING SYSTEM PERIARTICULAR PLATES
HOWMEDICA OSTEONICS CORP.         510(k) NO: K031959(SPECIAL)
ATTN: VIVIAN  KELLY               PHONE NO : 201-831-5581
59 ROUTE 17 SOUTH                 SE DECISION MADE: 25-JUL-03
ALLENDALE, NJ 07401-1677          510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: MODEL 780
HUDSON RESPIRATORY CARE, INC.     510(k) NO: K031383(SPECIAL)
ATTN: CHARLES  MIERKIEWICZ        PHONE NO : 909-676-5611
27711 DIAZ RD.                    SE DECISION MADE: 07-JUL-03
P.O. BOX 9020                     510(k) SUMMARY AVAILABLE FROM FDA
TEMECULA, CA 92589-9020

DEVICE: ICS MEDICAL CHARTR EP WITH ASSR AND CHARTR OAE SYSTEMS
ICS MEDICAL                       510(k) NO: K031986(SPECIAL)
ATTN: DELMAR F BLOEM              PHONE NO : 800-289-2150
125 COMMERCE DR.                  SE DECISION MADE: 24-JUL-03
SCHAUMBURG, IL 60173-5329         510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: DXAVIEW SPINE AND HIP, MODEL QCT-3D PLUS
IMAGE ANALYSIS, INC.              510(k) NO: K031991(SPECIAL)
ATTN: BEN  ARNOLD                 PHONE NO : 270-384-6400
1380 BURKESVILLE ST.              SE DECISION MADE: 30-JUL-03
COLUMBIA, KY 42728                510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: RUBELLACOL
IMMUNOSTICS, INC.                 510(k) NO: K031490(TRADITIONAL)
ATTN: JEFFREY  FLEISHMAN          PHONE NO : 732-918-0770
3505 SUNSET AVE.                  SE DECISION MADE: 16-JUL-03
OCEAN, NJ 07712                   510(k) STATEMENT

DEVICE: OSSEOTITE NT CERTAIN IMPLANTS
IMPLANT INNOVATIONS, INC.         510(k) NO: K031475(TRADITIONAL)
ATTN: JACQUELYN A HUGHES          PHONE NO : 561-776-6819
4555 RIVERSIDE DR.                SE DECISION MADE: 28-JUL-03
PALM BEACH GARDENS, FL 33410      510(k) SUMMARY AVAILABLE FROM FDA

 
DEVICE: HEDROCEL VERTEBRAL BODY REPLACEMENT, MODEL 06-172-00XX1
IMPLEX CORP.                      510(k) NO: K031823(SPECIAL)
ATTN: MARCI  HALEVI               PHONE NO : 201-818-1800
80 COMMERCE DR.                   SE DECISION MADE: 11-JUL-03
ALLENDALE, NJ 07401-1600          510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: HEMOSIL FACTOR IX DEFICIENT PLASMA
INSTRUMENTATION LABORATORY CO.    510(k) NO: K031829(TRADITIONAL)
ATTN: CAROL  MARBLE               PHONE NO : 781-861-4467
526 RT. 303                       SE DECISION MADE: 31-JUL-03
ORANGEBURG, NY 10962              510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: AUTION JET AJ-4270 URINE ANALYZER
INTERNATIONAL REMOTE IMAGING SYSTE510(k) NO: K030600(TRADITIONAL)
ATTN: CYNTHIA J.M.  NOLTE         PHONE NO : 508-643-0434
49 PLAIN ST.                      SE DECISION MADE: 11-JUL-03
NORTH ATTLEBORO, MA 02760         510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: ILT SAFE CROSS 0.035 SUPPORT CATHETER, MODEL C135SN1
INTRALUMINAL THERAPEUTICS, INC.   510(k) NO: K031417(TRADITIONAL)
ATTN: PAMELA  MISAJON             PHONE NO : 760-918-1820
6354 CORTE DEL ABETO              SE DECISION MADE: 11-JUL-03
SUITE A                           510(k) SUMMARY AVAILABLE FROM FDA
CARLSBAD, CA 92009

DEVICE: SAFE-CONNECT DRUG DISPENSING SPIKE, MODELS SC 4020, SC 4015, SC
INTRAVASCULAR INCORPORATED        510(k) NO: K031783(SPECIAL)
ATTN: STEVE  APERAVICH            PHONE NO : 847-596-7700
3600 BUR WOOD DR.                 SE DECISION MADE: 01-JUL-03
WAUKEGAN, IL 60085                510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: RH-900
IOMED, INC.                       510(k) NO: K031115(TRADITIONAL)
ATTN: CURTIS  JENSEN              PHONE NO : 801-975-1191
2441 SOUTH 3850 WEST, SUITE A     SE DECISION MADE: 10-JUL-03
SALT LAKE CITY, UT 84120-9941     510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: IVD CRYPTOSPORIDIUM ANTIGEN DETECTION ASSAY, MODEL CP-96
IVD RESEARCH, INC.                510(k) NO: K031059(TRADITIONAL)
ATTN: DAVE  LAMBILLOTTE           PHONE NO : 760-929-7744
5909 SEA LION PLACE, SUITE D      SE DECISION MADE: 10-JUL-03
CARLSBAD, CA 92008                510(k) SUMMARY AVAILABLE FROM FDA
                                  THIRD PARTY REVIEW

DEVICE: JASON MARINE ALL TERRAIN ELECTRIC WHEELCHAIR, MODEL SEEKER II
JASON MARINE ENTERPRISES, INC.    510(k) NO: K031342(ABBREVIATED)
ATTN: BRIAN  GAGNON               PHONE NO : 888-773-3537
4311 N.W. 64TH AVE.               SE DECISION MADE: 10-JUL-03
CORAL SPRINGS, FL 33067           510(k) STATEMENT

DEVICE: JMS EXTENSION SET WITH PLANECTA, PLANECTA (STAND ALONE UNIT), PL
JMS NORTH AMERICA CORP.           510(k) NO: K023668(TRADITIONAL)
ATTN: SWEE CHEAU  CHONG           PHONE NO : 510-888-9090
22320 FOOTHILL BLVD.,             SE DECISION MADE: 01-JUL-03
SUITE 350                         510(k) STATEMENT
HAYWARD, CA 94541

 
DEVICE: TRANSCRANIAL ELECTROTHERAPY STIMULATOR-A, MODEL TESA-1
KALACO SCIENTIFIC, INC.           510(k) NO: K024377(TRADITIONAL)
ATTN: GRACE  BARTOO               PHONE NO : 650-654-4484
131 GLENN WAY                     SE DECISION MADE: 21-JUL-03
SUITE 7                           510(k) SUMMARY AVAILABLE FROM FDA
SAN CARLOS, CA 94070

DEVICE: PROPHYPEARLS
KAVO AMERICA                      510(k) NO: K031868(SPECIAL)
ATTN: DANIEL  KAMM                PHONE NO : 847-374-1727
PO BOX 7007                       SE DECISION MADE: 09-JUL-03
DEER FIELD, IL 60015              510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: KAVO EVEREST ZS-BLANK MODELS, 42, 20, AND 60
KAVO AMERICA                      510(k) NO: K032081(SPECIAL)
ATTN: DANIEL  KAMM                PHONE NO : 847-374-1727
PO BOX 7007                       SE DECISION MADE: 24-JUL-03
DEER FIELD, IL 60015              510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: STAND OUT
KERR CORP.                        510(k) NO: K031484(TRADITIONAL)
ATTN: COLLEEN  BOSWELL            PHONE NO : 716-516-7484
1717 WEST COLLINS AVE.            SE DECISION MADE: 03-JUL-03
ORANGE, CA 92867                  510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: OPTIBOND FL
KERR DENTAL MATERIALS CENTER      510(k) NO: K031444(TRADITIONAL)
ATTN: COLLEEN  BOSWELL            PHONE NO : 714-516-7484
1717 WEST COLLINS AVE.            SE DECISION MADE: 02-JUL-03
ORANGE, CA 92867                  510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: ECHO SOUNDER, SINGLE-HANDED, MODEL ES-101EX
KOVEN TECHNOLOGY, INC.            510(k) NO: K031504(TRADITIONAL)
ATTN: J. HARVEY  KNAUSS           PHONE NO : 832-285-9423
11874 SOUTH EVELYN CIRCLE         SE DECISION MADE: 18-JUL-03
HOUSTON, TX 77071-3404            510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: KUANN DAH, COOL TANK MOTORIZED SCOOTER, KS4L320
KUANN DAH INDUSTRY CO., LTD.      510(k) NO: K031309(TRADITIONAL)
ATTN: KE-MIN  JEN                 PHONE NO : 886 3 5208829
NO. 58 FU-CHIUN ST.               SE DECISION MADE: 31-JUL-03
HSIN-CHU CITY, CHINA (TAIWAN)     510(k) STATEMENT

DEVICE: NANO TECH AND SUPER NANO ACUPUNCTURE NEEDLES
LHASA MEDICAL, INC.               510(k) NO: K031060(TRADITIONAL)
ATTN: KYUNG P RIIHIMAKI           PHONE NO : 781-335-5288
234 LIBBEY PKWY.                  SE DECISION MADE: 11-JUL-03
WEYMOUTH, MA 02189                510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: DBC PRESS ACUPUNCTURE NEEDLES
LHASA MEDICAL, INC.               510(k) NO: K031250(TRADITIONAL)
ATTN: KYUNG P RIIHIMAKI           PHONE NO : 781-340-1637
234 LIBBEY PKWY.                  SE DECISION MADE: 15-JUL-03
WEYMOUTH, MA 02189                510(k) SUMMARY AVAILABLE FROM FDA

 
DEVICE: 2.4 SMARTNAIL, MODELS 532416, 532425, 532435, 532445
LINVATEC BIOMATERIALS, LTD.       510(k) NO: K031981(SPECIAL)
ATTN: LAURA  KREJCI               PHONE NO : 727-399-5234
1311 CONCEPT BLVD                 SE DECISION MADE: 25-JUL-03
LARGO, FL 33773                   510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: LUMENIS FAMILY OF DISPOSABLE CONTACT TIP DELIVERY DEVICES
LUMENIS, LTD.                     510(k) NO: K030033(TRADITIONAL)
ATTN: ANNE  WORDEN                PHONE NO : 925-895-1200
2400 CONDENSA ST.                 SE DECISION MADE: 21-JUL-03
SANTA CLARA, CA 95051             510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: LUMENIS FAMILY OF IPL SYSTEMS AND COMBINATION IPL/ND:YAG SYSTEMS
LUMENIS, LTD.                     510(k) NO: K030342(TRADITIONAL)
ATTN: ANDREA L RUTH               PHONE NO : 408-764-3235
2400 CONDENSA ST.                 SE DECISION MADE: 17-JUL-03
SANTA CLARA, CA 95051             510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: MACROPORE OS RECONSTRUCTION
MACROPORE BIOSURGERY, INC.        510(k) NO: K024169(TRADITIONAL)
ATTN: KENNETH K KLEINHENZ         PHONE NO : 858-458-0900
6740 TOP GUN ST.                  SE DECISION MADE: 01-JUL-03
SAN DIEGO, CA 92121               510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: MAINLINE MAXIE HCG URINE PREGNANCY TEST
MAINLINE TECHNOLOGY, INC.         510(k) NO: K031445(TRADITIONAL)
ATTN: MARTHA  MAZUREK             PHONE NO : 734-930-2043
3985 RESEARCH PARK DR.            SE DECISION MADE: 01-JUL-03
ANN ARBOR, MI 48108               510(k) STATEMENT

DEVICE: OPTIBOLUS
MALLINCKRODT INC., LIEBEL-FLARSHEI510(k) NO: K031339(SPECIAL)
ATTN: ELLIS  ROGERS               PHONE NO : 513-948-4041
2111 EAST GALBRAITH RD.           SE DECISION MADE: 11-JUL-03
CINCINNATI, OH 45237              510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: PERSONAL DIGITAL WORKSTATION (PDW); FILM DIGITIZING CAMERA AND D
MAXXVISION, LLC                   510(k) NO: K031372(TRADITIONAL)
ATTN: JAMES K WALKER              PHONE NO : 352-378-6620
3014 NE 21ST WAY                  SE DECISION MADE: 02-JUL-03
GAINESVILLE, FL 32609             510(k) STATEMENT

DEVICE: MAYO CLINIC BC-10 1.5T
MAYO MEDICAL VENTURES             510(k) NO: K031119(ABBREVIATED)
ATTN: JADE  SADOSTY               PHONE NO : 507-284-8878
200 FIRST ST SW                   SE DECISION MADE: 15-JUL-03
ROCHESTER, MN 55905               510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: MAS TOX AMMONIA CONTROLLIQUID ASSAYED TOX AMMONIA CONTROL
MEDICAL ANALYSIS SYSTEMS, INC.    510(k) NO: K031392(TRADITIONAL)
ATTN: PENNY M LAYMAN              PHONE NO : 805-987-7891
5300 ADOLFO RD.                   SE DECISION MADE: 01-JUL-03
CAMARILLO, CA 93012               510(k) STATEMENT

 
DEVICE: URICHEMTRAK LIQUID ASSAYED URINE CONTROL
MEDICAL ANALYSIS SYSTEMS, INC.    510(k) NO: K031441(TRADITIONAL)
ATTN: PENNY M LAYMAN              PHONE NO : 805-987-7891
5300 ADOLFO RD.                   SE DECISION MADE: 01-JUL-03
CAMARILLO, CA 93012               510(k) STATEMENT

DEVICE: MAS BILIRUBIN LIQUID ASSAYED BILIRUBIN CONTROL
MEDICAL ANALYSIS SYSTEMS, INC.    510(k) NO: K031890(TRADITIONAL)
ATTN: PENNY M LAYMAN              PHONE NO : 805-987-7891
5300 ADOLFO RD.                   SE DECISION MADE: 16-JUL-03
CAMARILLO, CA 93012               510(k) STATEMENT

DEVICE: NGT
MEDICAL INNOVATIVE PRODUCTS       510(k) NO: K022558(TRADITIONAL)
ATTN: DEBBIE  IAMPIETRO           PHONE NO : 508-259-7374
7 TIFFANY TRAIL                   SE DECISION MADE: 08-JUL-03
HOPKINTON, MA 01748               510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: MIX2VIAL TRANSFER DEVICE
MEDIMOP MEDICAL PROJECTS, LTD.    510(k) NO: K031861(TRADITIONAL)
ATTN: BENNY  ARAZY                PHONE NO : 972 499 40337
MITZPE AVIV, INDUSTRIAL PK 13     SE DECISION MADE: 29-JUL-03
M.P. MISGAV, ISRAEL 20187         510(k) STATEMENT

DEVICE: SISS, INC. (D.B.A.MEDISISS) REPROCESSD ELECTROSURGICAL INSTRUMEN
MEDISISS                          510(k) NO: K030919(TRADITIONAL)
ATTN: MRRY ANN  BARKER            PHONE NO : 541-549-4164
723 CURTIS COURT                  SE DECISION MADE: 03-JUL-03
PO BOX 2060                       510(k) SUMMARY AVAILABLE FROM FDA
SISTERS, OR 97759                 THIRD PARTY REVIEW

DEVICE: MODIFICATION TO EVENCARE BLOOD GLUCOSE MONITORING SYSTEM
MEDLINE INDUSTRIES, INC.          510(k) NO: K031843(SPECIAL)
ATTN: ANDREA  HAFERKAMP           PHONE NO : 847-837-2759
ONE MEDLINE PL.                   SE DECISION MADE: 03-JUL-03
MUNDELEIN, IL 60060-4486          510(k) STATEMENT

DEVICE: MEDRAD SWABBABLE VALVE TRANSFER SET
MEDRAD, INC.                      510(k) NO: K031808(SPECIAL)
ATTN: ANDREW P ZELTWANGER         PHONE NO : 412-767-2400
ONE MEDRAD DR.                    SE DECISION MADE: 11-JUL-03
INDIANOLA, PA 15051               510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: VERDICT II, PROFILE II
MEDTOX DIAGNOSTICS, INC.          510(k) NO: K031032(SPECIAL)
ATTN: ALAN  MORRIS                PHONE NO : 336-226-6311
1238 ANTHONY RD.                  SE DECISION MADE: 14-JUL-03
BURLINGTON, NC 27215              510(k) STATEMENT

DEVICE: MC2X MULTI-STAGE VENOUS CANNULA
MEDTRONIC PERFUSION SYSTEMS       510(k) NO: K031776(SPECIAL)
ATTN: RONALD W BENNETT            PHONE NO : 763-391-9086
7611 NORTHLAND DR.                SE DECISION MADE: 25-JUL-03
MINNEAPOLIS, MN 55428             510(k) SUMMARY AVAILABLE FROM FDA

 
DEVICE: ULTRAFLEX VENOUS CANNULA, MODEL 970XX AND CB970XX
MEDTRONIC PERFUSION SYSTEMS       510(k) NO: K031827(SPECIAL)
ATTN: PREETI  JAIN                PHONE NO : 763-391-9000
7611 NORTHLAND DR.                SE DECISION MADE: 02-JUL-03
MINNEAPOLIS, MN 55428             510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: VERTE-STACK SPINAL SYSTEM
MEDTRONIC SOFAMOR DANEK           510(k) NO: K031780(SPECIAL)
ATTN: RICHARD  TREHARNE           PHONE NO : 901-396-3133
1800 PYRAMID PLACE                SE DECISION MADE: 30-JUL-03
MEMPHIS, TN 38132                 510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: MEDTRONIOC 7F LAUNCHER BIOPSY GUIDE CATHETER, MODEL LA7RVBB, MED
MEDTRONIC, INC.                   510(k) NO: K030671(TRADITIONAL)
ATTN: FRED L BOUCHER              PHONE NO : 978-777-0042
37A CHERRY HILL DR.               SE DECISION MADE: 31-JUL-03
DANVERS, MA                       510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: ATTAIN PREVAIL STEERABLE CATHETER SET, MODEL 6228CTH
MEDTRONIC, INC.                   510(k) NO: K031211(TRADITIONAL)
ATTN: LYNN  JENSEN                PHONE NO : 763-514-4459
7000 CENTRAL AVENUE NE            SE DECISION MADE: 17-JUL-03
MINNEAPOLIS, MN 55432-3576        510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: CARDIOBLATE BIPOLAR RADIOFREQUENCY SURGICAL ABLATION SYSTEM
MEDTRONIC, INC.                   510(k) NO: K031247(TRADITIONAL)
ATTN: SCOTT  CUNDY                PHONE NO : 763-391-9941
7601 NORTHLAND DR.                SE DECISION MADE: 17-JUL-03
MINNEAPOLIS, MN 55428             510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: MEGATECH SCIENTIFIC FACE MASK
MEGATECH SCIENTIFIC PTE LTD       510(k) NO: K030239(TRADITIONAL)
ATTN: CHIAM KIA  CHEE             PHONE NO : 65 656 57211
BLK 2 BUKIT BATOK STREET 24       SE DECISION MADE: 24-JUL-03
SKYTECH #09-03, SINGAPORE 659480  510(k) STATEMENT

DEVICE: MENTOR OBTAPE TRANS-OBTURATOR TAPE
MENTOR CORP.                      510(k) NO: K031767(TRADITIONAL)
ATTN: DONNA  CRAWFORD             PHONE NO : 805-879-6304
201 MENTOR DR.                    SE DECISION MADE: 17-JUL-03
SANTA BARBARA, CA 93111           510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: MINI STATCO2 CO2 DETECTOR, MODEL 10-55371
MERCURY MEDICAL                   510(k) NO: K031411(TRADITIONAL)
ATTN: WAYNE  GLOVER               PHONE NO : 800-237-6418
11300 49TH ST. NORTH              SE DECISION MADE: 30-JUL-03
CLEARWATER, FL 33762-4800         510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: SAPPHIRE DETACHABLE COIL SYSTEM
MICRO THERAPEUTICS, INC.          510(k) NO: K030392(TRADITIONAL)
ATTN: FLORIN  TRUUVERT            PHONE NO : 949-837-3700
2 GOODYEAR                        SE DECISION MADE: 21-JUL-03
IRVINE, CA 92618                  510(k) SUMMARY AVAILABLE FROM FDA

 
DEVICE: PCW PERCUTANEOUS COMPRESSION WIRE
MILLENNIUM MEDICAL TECHNOLOGIES, I510(k) NO: K031050(TRADITIONAL)
ATTN: DAVID W SCHLERF             PHONE NO : 925-356-2640
200 GREGORY LN.                   SE DECISION MADE: 14-JUL-03
SUITE C-100                       510(k) SUMMARY AVAILABLE FROM FDA
PLEASANT HILL, CA 94523-3389

DEVICE: MEDTRONIC MINIMED PARADIGM INSULIN PUMP, MODEL MMT-712
MINIMED, INC.                     510(k) NO: K031390(TRADITIONAL)
ATTN: MIRIELLE  MENGOTTO          PHONE NO : 818-362-5958
18000 DEVONSHIRE ST.              SE DECISION MADE: 23-JUL-03
NORTHRIDGE, CA 91325              510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: 4 FRENCH & 5 FRENCH ELECTROPHYSIOLOGY DIAGNOSTIC CATHETERS MODEL
MOGUL ENTERPRISES                 510(k) NO: K030852(SPECIAL)
ATTN: JAMIL  MOGUL                PHONE NO : 408-629-3340
6387 SAN IGNACIO AVE.             SE DECISION MADE: 10-JUL-03
SAN JOSE, CA 95119                510(k) STATEMENT

DEVICE: ELI 200+ AUDICOR
MORTARA INSTRUMENT, INC.          510(k) NO: K031182(TRADITIONAL)
ATTN: HARLAN L VAN MATRE          PHONE NO : 414-354-1600
7865 NORTH 86TH ST.               SE DECISION MADE: 25-JUL-03
MILWAUKEE, WI 53224               510(k) SUMMARY AVAILABLE FROM FDA
                                  THIRD PARTY REVIEW

DEVICE: MODEL J-5 MVO-MONITOR
MYOTRONICS-NOROMED, INC.          510(k) NO: K031998(SPECIAL)
ATTN: FRAY  ADIB                  PHONE NO : 206-243-4214
15425 53RD AVE. SOUTH             SE DECISION MADE: 24-JUL-03
TUKWILA, WA 98188                 510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: MYTECH / HAPPY LIFE BLOOD PRESSURE MONITOR
MYTECH TECHNOLOGY CO., LTD.       510(k) NO: K030221(TRADITIONAL)
ATTN: JEN  KE-MIN                 PHONE NO : 886 352 08829
NO. 58, FU-CHIUN ST.              SE DECISION MADE: 25-JUL-03
HSIN-CHU CITY, CHINA (TAIWAN)     510(k) STATEMENT

DEVICE: NEEDLETECH GUIDEWIRE INTRODUCER NEEDLE, MODELS 40021, 40069, 400
NEEDLETECH PRODUCTS, INC.         510(k) NO: K031173(TRADITIONAL)
ATTN: RICK  TRIPP                 PHONE NO : 508-431-4000
81 WEST ST.                       SE DECISION MADE: 23-JUL-03
ATTLEBORO, MA 02703               510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: NICHOLS ADVANTAGE ALDOSTERONE ASSAY
NICHOLS INSTITUTE DIAGNOSTICS     510(k) NO: K032188(TRADITIONAL)
ATTN: JIMMY  WONG                 PHONE NO : 949-940-7260
1311 CALLE BATIDO                 SE DECISION MADE: 31-JUL-03
SAN CLEMENTE, CA 92673            510(k) SUMMARY AVAILABLE FROM FDA
                                  THIRD PARTY REVIEW

DEVICE: CARBON FIBER BRIDGE, MODEL 28757
NOBEL BIOCARE AB                  510(k) NO: K031070(TRADITIONAL)
ATTN: ELIZABETH J MASON           PHONE NO : 714-282-4800
22725 SAVI RANCH PKWY.            SE DECISION MADE: 03-JUL-03
YORBA LINDA, CA 92887             510(k) SUMMARY AVAILABLE FROM FDA

 
DEVICE: ESTHETIC ZIRCONIA ABUTMENT
NOBEL BIOCARE AB                  510(k) NO: K031719(SPECIAL)
ATTN: ELIZABETH J MASON           PHONE NO : 714-282-4800
22715 SAVI RANCH PKWY.            SE DECISION MADE: 02-JUL-03
YORBA LINDA, CA 92887             510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: NOBEL DIRECT, MODELS 30937, 30938
NOBEL BIOCARE USA, INC.           510(k) NO: K031345(TRADITIONAL)
ATTN: ELIZABETH J MASON           PHONE NO : 714-282-4800
22715 SAVI RANCH PKWY.            SE DECISION MADE: 24-JUL-03
YORBA LINDA, CA 92887             510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: MODEL 9600, AVANT PULSE OXIMETER
NONIN MEDICAL, INC.               510(k) NO: K023044(TRADITIONAL)
ATTN: RICHARD P BENNETT           PHONE NO : 763-577-3166
2605 FERNBROOK LN. NORTH          SE DECISION MADE: 23-JUL-03
PLYMOUTH, MN 55447-4755           510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: PROVIDENCE MOLDING HELMET
NORTHEAST ORTHOTICS AND PROTHETICS510(k) NO: K030669(ABBREVIATED)
ATTN: D. BARRY  MCCOY             PHONE NO : 401-444-5477
170 MACKLIN STREET                SE DECISION MADE: 18-JUL-03
CRANSTON, RI 02920                510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: NXSTAGE SYSTEM ONE
NXSTAGE MEDICAL, INC.             510(k) NO: K030470(TRADITIONAL)
ATTN: NORMA  LEMAY                PHONE NO : 978-687-4700
439 SOUTH UNION ST.               SE DECISION MADE: 07-JUL-03
SUITE 501                         510(k) SUMMARY AVAILABLE FROM FDA
LAWRENCE, MA 01843                THIRD PARTY REVIEW

DEVICE: HYDROGENICS 2.0 60 UV ASPHERE (OCUFILCON F) SOFT (HYDROPHILIC) C
OCULAR SCIENCES, INC.             510(k) NO: K031477(ABBREVIATED)
ATTN: RICHARD E LIPPMAN           PHONE NO : 240-683-3738
15825 SHADY GROVE RD, SUITE 30    SE DECISION MADE: 18-JUL-03
ROCKVILLE, MD 20850               510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: VISERA RHINO-LARYNGOVIDEOSCOPE OLYMPUS ENF TYPE V
OLYMPUS OPTICAL CO., LTD.         510(k) NO: K031648(TRADITIONAL)
ATTN: TINA  STEFFANIE-OAK         PHONE NO : 631-844-5477
TWO CORPORATE CENTER DR.          SE DECISION MADE: 24-JUL-03
MELVILLE, NY 11747-3157           510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: OLYMPUS XCYF-TP3 CYSTOFIBERSCOPE/NEPHROFIBERSCOPE
OLYMPUS OPTICAL CO., LTD.         510(k) NO: K032092(TRADITIONAL)
ATTN: MASAO  WADA                 PHONE NO : 814 264 22891
34-3 HIRAI HINODE-MACHI,          SE DECISION MADE: 16-JUL-03
NISHITAMA-GUN, TOKYO, JAPAN 190-01510(k) SUMMARY AVAILABLE FROM FDA
                                  THIRD PARTY REVIEW

DEVICE: XSIF-1TQ140A SMALL INTESTINAL VIDEOSCOPE
OLYMPUS OPTO-ELECTRONICS CO., LTD.510(k) NO: K031256(TRADITIONAL)
ATTN: TINA  STEFFANIE-OAK         PHONE NO : 631-844-5477
TWO CORPORATE CENTER DR.          SE DECISION MADE: 23-JUL-03
MELVILLE, NY 11747-3157           510(k) SUMMARY AVAILABLE FROM FDA

 
DEVICE: REUSABLE SMARTSTITCH SUTURE DEVICE, MODELS OM-8007, OM-8500
OPUS MEDICAL, INC.                510(k) NO: K030170(TRADITIONAL)
ATTN: JAMES W HART                PHONE NO : 949-234-0400
27127 CALLE ARROYO, SUITE 1924    SE DECISION MADE: 28-JUL-03
SAN JUAN CAPISTRANO, CA 92675     510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: LIFEPORT, KIDNEY PERFUSION TRANSPORTER (KTR)
ORGAN RECOVERY SYSTEMS, INC.      510(k) NO: K021362(TRADITIONAL)
ATTN: STANLEY J HARRIS            PHONE NO : 843-722-6657
701 EAST BAY ST.                  SE DECISION MADE: 31-JUL-03
SUITE 433                         510(k) STATEMENT
CHARLESTON, SC 29403

DEVICE: ORTHO DEVELOPMENT BALANCED KNEE MODULAR TIBIAL SYSTEM
ORTHO DEVELOPMENT CORP.           510(k) NO: K031201(TRADITIONAL)
ATTN: NADEEM  AHMED               PHONE NO : 801-553-9991
12187 SOUTH BUSINESS PARK DR.     SE DECISION MADE: 15-JUL-03
DRAPER, UT 84020                  510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: EXTENDERS BGS GRANULES, CUBES, BLOCKS, AND PLUGS
OSTEOBIOLOGICS, INC.              510(k) NO: K030288(TRADITIONAL)
ATTN: GABRIELE G NEIDERAUER       PHONE NO : 210-690-2131
UNIVERSITY BUSINESS PARK          SE DECISION MADE: 17-JUL-03
12500 NETWORK, SUITE 112          510(k) SUMMARY AVAILABLE FROM FDA
SAN ANTONIO, TX 78249-3308

DEVICE: TEMPORARY RESIN CEMENT
PARKELL, INC.                     510(k) NO: K031212(TRADITIONAL)
ATTN: NELSON J GENDUSA            PHONE NO : 631-249-1134
155 SCHMITT BLVD.                 SE DECISION MADE: 11-JUL-03
P.O. BOX 376                      510(k) SUMMARY AVAILABLE FROM FDA
FARMINGDALE, NY 11735

DEVICE: PASCO MIC AND MIC/ID PANELS, GEMIFLOXACIN
PASCO LABORATORIES, INC.          510(k) NO: K031727(TRADITIONAL)
ATTN: LINDA K DILLON              PHONE NO : 303-390-3240
12750 WEST 42ND AVE.              SE DECISION MADE: 30-JUL-03
WHEAT RIDGE, CO 80033             510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: SHOCKWAVE SUSPENSION WHEELCHAIR
PER4MAX MEDICAL, LLC              510(k) NO: K032123(TRADITIONAL)
ATTN: TIM  CRISWELL               PHONE NO : 972-641-6773
2550 114TH ST., SUITE 190         SE DECISION MADE: 31-JUL-03
GRAND PRAIRIE, TX 75050           510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: SECQUIRE CELL SEPARATOR
PERFUSION PARTNERS & ASSOC. INC.  510(k) NO: K024080(TRADITIONAL)
ATTN: E.J.  SMITH                 PHONE NO : 888-729-9674
P.O. BOX 4341                     SE DECISION MADE: 02-JUL-03
CROFTON, MD 21114                 510(k) STATEMENT

DEVICE: PHILIPS COMPURECORD PERI-OPERATIVE INFORMATION SYSTEM SOFTWARE
PHILIPS MEDICAL SYSTEMS           510(k) NO: K030939(SPECIAL)
ATTN: JUDITH K PHILLIPS           PHONE NO : 412-279-3263
1082 BOWER HILL RD.               SE DECISION MADE: 15-JUL-03
PITTSBURGH, PA 15243              510(k) SUMMARY AVAILABLE FROM FDA

 
DEVICE: PICOSAT II SPO2 PULSE OXIMETRY MODULE
PHILIPS MEDICAL SYSTEMS           510(k) NO: K030973(SPECIAL)
ATTN: DAVID  OSBORN               PHONE NO : 978-659-3178
3000 MINUTEMAN RD.                SE DECISION MADE: 23-JUL-03
ANDOVER, MA 01810-1099            510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: PHILIPS PAGE WRITER TRIM SERIES CARDIOGRAPH INCLUDING I, II, III
PHILIPS MEDICAL SYSTEMS           510(k) NO: K031422(ABBREVIATED)
ATTN: SONGHUA  ZHANG              PHONE NO : 978-659-7319
3000 MINUTEMAN RD.                SE DECISION MADE: 03-JUL-03
ANDOVER, MA 01810-1099            510(k) SUMMARY AVAILABLE FROM FDA
                                  THIRD PARTY REVIEW

DEVICE: PHILIPS VIEWFORUM 2003
PHILIPS MEDICAL SYSTEMS           510(k) NO: K032096(TRADITIONAL)
ATTN: LYNN T HARMER               PHONE NO : 425-487-7312
22100 BOTHELL EVERETT HWY         SE DECISION MADE: 18-JUL-03
P.O. BOX 3003                     510(k) SUMMARY AVAILABLE FROM FDA
BOTHELL, WA 98041-8431            THIRD PARTY REVIEW

DEVICE: PHILIPS TRACEMASTER ECG MANAGEMENT SYSTEM, MODELS M5100A AND M51
PHILIPS MEDICAL SYSTEMS           510(k) NO: K032103(SPECIAL)
ATTN: SONGHUA  ZHANG              PHONE NO : 978-659-7319
3000 MINUTEMAN RD.                SE DECISION MADE: 22-JUL-03
ANDOVER, MA 01810                 510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: DUNLEE "FORMAT" COLLIMATOR FAMILY
PHILIPS MEDICAL SYSTEMS NORTH AMER510(k) NO: K031597(TRADITIONAL)
ATTN: LYNN  HARMER                PHONE NO : 425-487-7312
22100 BOTHELL EVERETT HWY.        SE DECISION MADE: 21-JUL-03
P.O. BOX 3003                     510(k) SUMMARY AVAILABLE FROM FDA
BOTHELL, WA 98041-3003

DEVICE: PHILLIPS OMNIDIAGNOST ELEVA
PHILIPS MEDICAL SYSTEMS NORTH AMER510(k) NO: K032046(TRADITIONAL)
ATTN: LYNN  HARMER                PHONE NO : 425-487-7312
22100 BOTHELL EVERETT HWY.        SE DECISION MADE: 17-JUL-03
P.O. BOX 3003                     510(k) SUMMARY AVAILABLE FROM FDA
BOTHELL, WA 98041-3003            THIRD PARTY REVIEW

DEVICE: GEMINI 16
PHILIPS MEDICAL SYSTEMS(CLEVELAND)510(k) NO: K032036(TRADITIONAL)
ATTN: CHRISTOF  LITTWITZ          PHONE NO : 440-483-3585
595 MINER RD.                     SE DECISION MADE: 11-JUL-03
CLEVELAND, OH 44143               510(k) SUMMARY AVAILABLE FROM FDA
                                  THIRD PARTY REVIEW

DEVICE: OMNILUX RED
PHOTO THERAPEUTICS LIMITED        510(k) NO: K030426(TRADITIONAL)
ATTN: MAUREEN  O'CONNELL          PHONE NO : 978-207-1245
5 TIMBER LN.                      SE DECISION MADE: 17-JUL-03
NORTH READING, MA 01864           510(k) SUMMARY AVAILABLE FROM FDA

 
DEVICE: UC-PLUS SOLUTION UNICONDYLAR KNEE
PLUS ORTHOPEDICS                  510(k) NO: K032052(SPECIAL)
ATTN: J.D.  WEBB                  PHONE NO : 512-388-0199
1001 OAKWOOD BLVD.                SE DECISION MADE: 25-JUL-03
ROUND ROCK, TX 78681-2700         510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: COMPPAC VENTILATOR MODELS 200 & PS11 POWER SUPPLY/CHARGER
PNEU PAC, LTD.                    510(k) NO: K021841(TRADITIONAL)
ATTN: DONALD  ALEXANDER           PHONE NO : 262-542-3100
SMITHS MEDICAL                    SE DECISION MADE: 17-JUL-03
N7 W22025 JOHNSON ROAD            510(k) SUMMARY AVAILABLE FROM FDA
WAUKESHA, WI 53186-1856

DEVICE: PER-FIT PERCUTANEOUS DILATIONAL TRACHEOSTOMY KIT
PORTEX, INC.                      510(k) NO: K031057(TRADITIONAL)
ATTN: TIMOTHY J TALCOTT           PHONE NO : 603-352-3812
10 BOWMAN DR.                     SE DECISION MADE: 18-JUL-03
KEENE, NH 03431                   510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: GLOVETEX POWDER FREE LATEX EXAMINATION GLOVES, BLUE, NON-STERILE
PT. WRP BUANA MULTICORPORA        510(k) NO: K032007(TRADITIONAL)
ATTN: NG POY  SIN                 PHONE NO : 061 694 2461
JALAN JERMAL #20B, KELURAHAN      SE DECISION MADE: 28-JUL-03
SEI MATI, MEDAN LABUHAN KM 17     510(k) SUMMARY AVAILABLE FROM FDA
MEDAN, INDONESIA 20252

DEVICE: FASTPACK FREE T4 IMMUNOASSAY
QUALIGEN, INC.                    510(k) NO: K030329(TRADITIONAL)
ATTN: DOROTHY  DEINZER            PHONE NO : 760-918-9165
2042 CORTE DEL NOGAL              SE DECISION MADE: 03-JUL-03
CARLSBAD, CA 92009-1410           510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: RADIUS 018 COUGAR WIRE
RADIUS MEDICAL TECHNOLOGIES, INC. 510(k) NO: K032129(SPECIAL)
ATTN: DEBBIE  IAMPIETRO           PHONE NO : 508-435-9893
7 TIFFANY TRAIL                   SE DECISION MADE: 17-JUL-03
HOPKINTON, MA 01748               510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: XPECT INFLUENZA A/B
REMEL INC                         510(k) NO: K031565(TRADITIONAL)
ATTN: MARY ANN  SILVIUS           PHONE NO : 913-895-4054
12076 SANTA FE DRIVE              SE DECISION MADE: 17-JUL-03
LENEXA, KS 66215                  510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: S7 ELITE AND AUTOSET SPIRIT CPAP SYSTEMS WITH RESLINK
RESMED LTD.                       510(k) NO: K024191(TRADITIONAL)
ATTN: ROGER  KOTTER               PHONE NO : 858-746-2282
14040 DANIELSON ST.               SE DECISION MADE: 02-JUL-03
POWAY, CA 92064-6857              510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: BIPAP HARMONY VENTILATORY SUPPORT SYSTEM
RESPIRONICS, INC.                 510(k) NO: K031656(SPECIAL)
ATTN: ZITA A YURKO                PHONE NO : 724-387-4120
1001 MURRY RIDGE LN.              SE DECISION MADE: 30-JUL-03
MURRYSVILLE, PA 15668             510(k) SUMMARY AVAILABLE FROM FDA

 
DEVICE: RITA MODEL 1500X ELECTROSURGICAL RF GENERATOR AND ACCESSORIES (E
RITA MEDICAL SYSTEMS INC          510(k) NO: K031926(SPECIAL)
ATTN: ERIN  MAZZONE               PHONE NO : 650-314-3400
967 N. SHORELINE BLVD.            SE DECISION MADE: 17-JUL-03
MOUNTAIN VIEW, CA 94043           510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: FERRITIN GENERATION 2
ROCHE DIAGNOSTICS CORP.           510(k) NO: K031650(TRADITIONAL)
ATTN: KAY A TAYLOR                PHONE NO : 317-521-3544
9115 HAGUE RD.                    SE DECISION MADE: 17-JUL-03
INDIANAPOLIS, IN 46250            510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: ACCU-CHEK COMPACT TEST STRIP
ROCHE DIAGNOSTICS CORP.           510(k) NO: K031755(SPECIAL)
ATTN: SCOTT  THIEL                PHONE NO : 800-428-5074
9115 HAGUE RD.                    SE DECISION MADE: 03-JUL-03
INDIANAPOLIS, IN 46250            510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: COBAS INTEGRA CHOLESTEROL GEN. 2
ROCHE DIAGNOSTICS CORP.           510(k) NO: K031824(SPECIAL)
ATTN: SHERRI L COENEN             PHONE NO : 317-521-3831
9115 HAGUE RD.                    SE DECISION MADE: 09-JUL-03
INDIANAPOLIS, IN 46250            510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: COBAS INTEGRA CARBON DIOXIDE ASSAY
ROCHE DIAGNOSTICS CORP.           510(k) NO: K031879(SPECIAL)
ATTN: SHERRI L COENEN             PHONE NO : 317-521-3831
9115 HAGUE RD.                    SE DECISION MADE: 17-JUL-03
INDIANAPOLIS, IN 46250            510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: AMMONIA/ETHANOL/CO2 CALIBRATOR, CONTROL NORMAL, CONTROL ABNORMAL
ROCHE DIAGNOSTICS CORP.           510(k) NO: K031880(SPECIAL)
ATTN: SHERRI L COENEN             PHONE NO : 317-521-3831
9115 HAGUE RD.                    SE DECISION MADE: 16-JUL-03
INDIANAPOLIS, IN 46250            510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: ROCHE DIAGNOSTICS ELECSYS PRECICONTROL CARDIAC
ROCHE DIAGNOSTICS CORP.           510(k) NO: K032089(SPECIAL)
ATTN: SHERRI L COENEN             PHONE NO : 317-521-3831
9115 HAGUE RD.                    SE DECISION MADE: 30-JUL-03
INDIANAPOLIS, IN 46250            510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: MR FIBER OPTIC ECG GATING SYSTEM
SA INSTRUMENTS, INC.              510(k) NO: K031731(TRADITIONAL)
ATTN: G. RONALD  MORRIS           PHONE NO : 631-689-9804
65 MAIN STREET                    SE DECISION MADE: 30-JUL-03
STONY BROOK, NY 11790             510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: SAUFLON MULTIPURPOSE SOLUTION - NO RUB
SAUFLON PHARMACEUTICALS, LTD.     510(k) NO: K030278(TRADITIONAL)
ATTN: LIGIA  DELACRUZ             PHONE NO : 44 208 3224200
49-53 YORK ST.                    SE DECISION MADE: 30-JUL-03
TWICKENHAM, MIDDLESEX, UNITED KING510(k) SUMMARY AVAILABLE FROM FDA

 
DEVICE: CYCLASE ACTIVATING PTH (CAP) IMMUNORADIOMETRIC (IRMA) ASSAY KIT,
SCANTIBODIES LABORATORY, INC.     510(k) NO: K031534(TRADITIONAL)
ATTN: RICHARD  LENART             PHONE NO : 619-258-9300
9336 ABRAHAM WAY                  SE DECISION MADE: 30-JUL-03
SANTEE, CA 92071                  510(k) STATEMENT

DEVICE: UCR SPINAL SYSTEM, LAMINAR HOOKS, PEDICLE HOOKS, AND INSTRUMENTS
SEASPINE                          510(k) NO: K031381(TRADITIONAL)
ATTN: DIANA  SMITH                PHONE NO : 619-251-9132
727 PARK BLVD.                    SE DECISION MADE: 30-JUL-03
SAN DIEGO, CA 92101               510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: SEZ SAFETY SYRINGE
SEZ CORPORATION                   510(k) NO: K031163(TRADITIONAL)
ATTN: DANIEL  KAMM                PHONE NO : 847-374-1727
PO 7007                           SE DECISION MADE: 08-JUL-03
DEERFIELD, IL 60015               510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: VINYL EXAM GLOVES, POWDER-FREE, YELLOW
SHANGHAI JIAWANG INDUSTRIAL CO. LT510(k) NO: K031854(TRADITIONAL)
ATTN: JANNA P TUCKER              PHONE NO : 775-342-2612
198 AVENUE DE LA D'EMERALD        SE DECISION MADE: 25-JUL-03
SPARKS, NV 89434-9550             510(k) STATEMENT

DEVICE: GLASIONOMER FX-II
SHOFU DENTAL CORP.                510(k) NO: K031467(TRADITIONAL)
ATTN: ROBERT  NOBLE               PHONE NO : 760-736-3277
1225 STONE DR.                    SE DECISION MADE: 17-JUL-03
SAN MARCOS, CA 92069-4059         510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: ACUSON CV70 CARDIOVASCULAR SYSTEM
SIEMENS MEDICAL SOLUTIONS USA, INC510(k) NO: K032111(TRADITIONAL)
ATTN: CAREY  CHAVEZ               PHONE NO : 425-557-1683
22010 S.E. 51ST ST.               SE DECISION MADE: 18-JUL-03
ISSAQUAH, WA 98029-7298           510(k) SUMMARY AVAILABLE FROM FDA
                                  THIRD PARTY REVIEW

DEVICE: SEQUOIA 8.0 DIAGNOSTIC ULTRASOUND SYSTEM
SIEMENS MEDICAL SOLUTIONS USA, INC510(k) NO: K032114(TRADITIONAL)
ATTN: JERRY W TSUTSUMI            PHONE NO : 650-943-7286
1230 SHOREBIRD WAY                SE DECISION MADE: 21-JUL-03
P O BOX 7393                      510(k) SUMMARY AVAILABLE FROM FDA
MOUNTAIN VIEW, CA 94039-7393      THIRD PARTY REVIEW

DEVICE: PEEK TETRIS SPINAL IMPLANT
SIGNUS MEDICAL LLC.               510(k) NO: K031757(SPECIAL)
ATTN: AL  ALEXANDER               PHONE NO : 763-287-3830
4050 OLSON MEMORIAL HIGHWAY       SE DECISION MADE: 30-JUL-03
SUITE 350                         510(k) SUMMARY AVAILABLE FROM FDA
MINNEAPOLIS, MN 55422

DEVICE: SINCLAIR WOUND AND SKIN EMULSION
SINCLAIR PHARMACEUTICALS, LTD.    510(k) NO: K024367(TRADITIONAL)
ATTN: MICHAEL  KILLEEN            PHONE NO : 441 483 428611
BOROUGH RD.                       SE DECISION MADE: 28-JUL-03
GODALMING, SURREY, UNITED KINGDOM 510(k) SUMMARY AVAILABLE FROM FDA

 
DEVICE: OXINIUM FEMORAL HEADS
SMITH & NEPHEW, INC.              510(k) NO: K030766(SPECIAL)
ATTN: KIM P KELLY                 PHONE NO : 901-399-6566
1450 E. BROOKS RD.                SE DECISION MADE: 25-JUL-03
MEMPHIS, TN 38116                 510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: EXTERNAL FIXATION SYSTEMS
SMITH & NEPHEW, INC.              510(k) NO: K031181(TRADITIONAL)
ATTN: DAVID  HENLEY               PHONE NO : 901-399-6487
1450 E. BROOKS RD.                SE DECISION MADE: 14-JUL-03
MEMPHIS, TN 38116                 510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: TAG ROD BIORAPTOR SUTURE ANCHOR 7209317, 7209318
SMITH & NEPHEW, INC.              510(k) NO: K031685(SPECIAL)
ATTN: JASON  BILOBRAM             PHONE NO : 508-261-3699
130 FORBES BLVD.                  SE DECISION MADE: 01-JUL-03
MANSFIELD, MA 02048               510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: SCANLUBE
SONOTECH, INC.                    510(k) NO: K031222(TRADITIONAL)
ATTN: MARGARET J LARSON           PHONE NO : 360-671-9121
774 MARINE DR.                    SE DECISION MADE: 23-JUL-03
BELLINGHAM, WA 98225              510(k) STATEMENT

DEVICE: SCANTEC PAD
SONOTECH, INC.                    510(k) NO: K031894(SPECIAL)
ATTN: MARGARET J LARSON           PHONE NO : 360-671-9121
774 MARINE DR.                    SE DECISION MADE: 18-JUL-03
BELLINGHAM, WA 98225              510(k) STATEMENT

DEVICE: BENCO SPHERICAL
SOUTHERN DENTAL INDUSTRIES, INC.  510(k) NO: K031658(TRADITIONAL)
ATTN: SAMANTHA J CHEETHAM         PHONE NO : 630-238-8300
729 N. ROUTE 83, SUITE 315        SE DECISION MADE: 29-JUL-03
BENSENVILLE, IL 60106             510(k) STATEMENT

DEVICE: SPINAL CONCEPTS, INC. BACFIX TI SPINAL SYSTEM
SPINAL CONCEPTS, INC.             510(k) NO: K030087(ABBREVIATED)
ATTN: LISA  PETERSON              PHONE NO : 512-918-2700
5301 RIATA PARK COURT             SE DECISION MADE: 17-JUL-03
BLDG F                            510(k) SUMMARY AVAILABLE FROM FDA
AUSTIN, TX 78727

DEVICE: MODIFICATION TO FORTITUDE CEMENT RESTRICTOR
SPINAL CONCEPTS, INC.             510(k) NO: K031837(SPECIAL)
ATTN: LISA  PETERSON              PHONE NO : 512-533-1080
5301 RIATA PARK CT., BLDG. F      SE DECISION MADE: 24-JUL-03
AUSTIN, TX 78727                  510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: ORLON NONABSORABLE SURGICAL SUTURE USP
SRI ORION PHARMACEUTICALS & SUTURE510(k) NO: K030177(ABBREVIATED)
ATTN: NORMAN F ESTRIN             PHONE NO : 301-279-2899
9109 COPENHAVER DR.               SE DECISION MADE: 21-JUL-03
POTOMAC, MD 20854                 510(k) SUMMARY AVAILABLE FROM FDA

 
DEVICE: APEEL CS CATHETER DELIVERY SYSTEM
ST. JUDE MEDICAL                  510(k) NO: K031906(SPECIAL)
ATTN: MIKE  BURNSIDE              PHONE NO : 952-933-4700
14901 DEVEAU PL.                  SE DECISION MADE: 18-JUL-03
MINNETONKA, MN 55345-2126         510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: STELLARTECH COAGULATION SYSTEM, MODELS  (1100C-115 & 1100C-230)
STELLARTECH RESEARCH CORP.        510(k) NO: K032062(SPECIAL)
ATTN: JAMES R SANTOS              PHONE NO : 408-331-3000
1346 BORDEAUX DR.                 SE DECISION MADE: 29-JUL-03
SUNNYVALE, CA 94089               510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: ITI DENTAL IMPLANT SYSTEM
STRAUMANN USA                     510(k) NO: K031055(TRADITIONAL)
ATTN: LINDA  JALBERT              PHONE NO : 781-890-0001
RESERVOIR PLACE,                  SE DECISION MADE: 07-JUL-03
1601 TRAPELO ROAD                 510(k) SUMMARY AVAILABLE FROM FDA
WALTHAM, MA 02154

DEVICE: THE SUAD DEVICE
STRONG DENTAL INC.                510(k) NO: K023836(ABBREVIATED)
ATTN: CLYDE A TAKEGUCHI           PHONE NO : 703-406-0906
21525 RIDGETOP CIRCLE             SE DECISION MADE: 08-JUL-03
SUITE 320                         510(k) SUMMARY AVAILABLE FROM FDA
STERLING, VA 20166

DEVICE: MODIFICATION TO STRYKER PAINPUMP
STRYKER INSTRUMENTS               510(k) NO: K031249(TRADITIONAL)
ATTN: NICOLE  PETTY               PHONE NO : 269-323-7700
4100 EAST MILHAM AVE.             SE DECISION MADE: 21-JUL-03
KALAMAZOO, MI 49001               510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: SUNDER CENTRAL VENOUS CATHETER KIT, MODELS SD-3L55F30J AND SD-3L
SUNDER BIOMEDICAL TECH. CO., LTD. 510(k) NO: K024007(TRADITIONAL)
ATTN: TONY  HUNG                  PHONE NO : 886 4 23755650
10F-1, 1-67, WU-CHUAN RD.         SE DECISION MADE: 14-JUL-03
TAICHUNG CITY, CHINA (TAIWAN) 403 510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: SPARTAN ORTHOPAEDIC WRIST BRACE, MODEL SCT-1
SURGITECH, INC.                   510(k) NO: K031576(TRADITIONAL)
ATTN: CHRISTOPHER  CROWELL        PHONE NO : 760-450-0194
2424 VISTA WAY, SUITE 300         SE DECISION MADE: 31-JUL-03
OCEANSIDE, CA 92054               510(k) STATEMENT

DEVICE: SURGRX ENSEAL VESSEL SEALING AND HEMOSTASIS SYSTEM INCLUDING THE
SURGRX INC                        510(k) NO: K031133(TRADITIONAL)
ATTN: LINDA  OLESON               PHONE NO : 650-938-0424
2629-B TERMINAL BLVD.             SE DECISION MADE: 03-JUL-03
MOUNTAIN VIEW, CA 94043           510(k) SUMMARY AVAILABLE FROM FDA
                                  THIRD PARTY REVIEW

DEVICE: DERMOSONIC NON-INVASIVE SUBDERMAL THERAPY SYSTEM
SYBARITIC, INC.                   510(k) NO: K024307(TRADITIONAL)
ATTN: RANDALL E BERGLUND          PHONE NO : 952-703-5369
9220 JAMES AVE. SOUTH             SE DECISION MADE: 02-JUL-03
BLOOMINGTON, MN 55431             510(k) STATEMENT

 
DEVICE: FILL-IN
SYBRON DENTAL SPECIALTIES, INC.   510(k) NO: K031476(TRADITIONAL)
ATTN: COLLEEN  BOSWELL            PHONE NO : 714-516-7484
1717 W. COLLINS AVE.              SE DECISION MADE: 02-JUL-03
ORANGE, CA 92867                  510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: SYNTHES ANTERIOR CERVICAL LOCKING PLATE (ACLP) SYSTEM
SYNTHES (USA)                     510(k) NO: K031276(TRADITIONAL)
ATTN: JON  GILBERT                PHONE NO : 484-356-9615
1690 RUSSELL RD.                  SE DECISION MADE: 02-JUL-03
PAOLI, PA 19301                   510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: SYNTHES (USA) COMPARTMENTAL PRESSURE MONITORING SYSTEM
SYNTHES (USA)                     510(k) NO: K031555(TRADITIONAL)
ATTN: LISA M BOYLE                PHONE NO : 610-647-9700
1690 RUSSELL RD.                  SE DECISION MADE: 08-JUL-03
P.O. BOX 1766                     510(k) SUMMARY AVAILABLE FROM FDA
PAOLI, PA 19301

DEVICE: SYNTHES SMALL COBINATION CLAMP-MR SAFE
SYNTHES (USA)                     510(k) NO: K031724(TRADITIONAL)
ATTN: BONNIE  SMITH               PHONE NO : 610-647-9700
1690 RUSSELL RD.                  SE DECISION MADE: 14-JUL-03
PAOLI, PA 19301                   510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: SYNTHES LOW PROFILE NEURO SYSTEM - 3 MM SCREWS
SYNTHES (USA)                     510(k) NO: K031807(SPECIAL)
ATTN: BONNIE J SMITH              PHONE NO : 610-647-9700
1690 RUSSELL RD.                  SE DECISION MADE: 02-JUL-03
PAOLI, PA 19301                   510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: TAGA VELOCITY HUMIDIFIER
TAGA MEDICAL TECHNOLOGIES, INC.   510(k) NO: K031179(TRADITIONAL)
ATTN: GARY  AUSTIN                PHONE NO : 440-602-8242
34675 VOKES DR STE 105            SE DECISION MADE: 17-JUL-03
EASTLAKE, OH 44095                510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: C. DIFF CHEK - 30
TECHLAB, INC.                     510(k) NO: K030991(TRADITIONAL)
ATTN: DAVID M LYERLY              PHONE NO : 540-953-1664
1861 PRATT DR., STE. 1030         SE DECISION MADE: 11-JUL-03
BLACKSBURG, VA 24060-6364         510(k) STATEMENT

DEVICE: C. DIFF CHEK - 60
TECHLAB, INC.                     510(k) NO: K030992(TRADITIONAL)
ATTN: DAVID M LYERLY              PHONE NO : 540-953-1664
1861 PRATT DR., STE. 1030         SE DECISION MADE: 11-JUL-03
BLACKSBURG, VA 24060-6364         510(k) STATEMENT

DEVICE: MX 300 OXYGEN MONITOR
TELEDYNE ANALYTICAL INSTRUMENTS   510(k) NO: K024155(TRADITIONAL)
ATTN: RAY  KHAJAVI                PHONE NO : 626-934-1502
16830 CHESTNUT ST.                SE DECISION MADE: 17-JUL-03
CITY OF INDUSTRY, CA 91749        510(k) STATEMENT

 
DEVICE: RX300 OXYGEN ANALYZER
TELEDYNE ANALYTICAL INSTRUMENTS   510(k) NO: K024228(TRADITIONAL)
ATTN: RAY  KHAJAVI                PHONE NO : 626-934-1502
16830 CHESTNUT ST.                SE DECISION MADE: 17-JUL-03
CITY OF INDUSTRY, CA 91749        510(k) STATEMENT

DEVICE: TELZUIT CARDIAC MONITORING SYSTEM
TELZUIT TECHNOLOGIES, INC.        510(k) NO: K031229(ABBREVIATED)
ATTN: CYNTHIA J.M.  NOLET         PHONE NO : 919-859-4207
49 PLAIN ST.                      SE DECISION MADE: 09-JUL-03
NORTH ATTLEBORO, MA 02760         510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: VIRTUOSAPH
TERUMO CARDIOVASCULAR SYSTEMS CORP510(k) NO: K031891(TRADITIONAL)
ATTN: KIM  AVES                   PHONE NO : 800-262-3304
6200 JACKSON RD.                  SE DECISION MADE: 29-JUL-03
ANN ARBOR, MI 48103               510(k) SUMMARY AVAILABLE FROM FDA
                                  THIRD PARTY REVIEW

DEVICE: TERUMO SURGUARD 2 SAFETY NEEDLE
TERUMO MEDICAL CORP.              510(k) NO: K031453(TRADITIONAL)
ATTN: BARBARA  SMITH              PHONE NO : 410-392-7241
950 ELKTON BLVD.                  SE DECISION MADE: 08-JUL-03
ELKTON, MD 21921                  510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: FREELITE HUMAN KAPPA AND LAMBDA FREE KITS FOR USE ON THE DAD BEH
THE BINDING SITE, LTD.            510(k) NO: K031016(TRADITIONAL)
ATTN: JAY H GELLER                PHONE NO : 310-449-1399
WEST TOWER, SUITE 4000            SE DECISION MADE: 15-JUL-03
2425 WEST OLYMPIC BOULEVARD       510(k) SUMMARY AVAILABLE FROM FDA
SANTA MONICA, CA 90404

DEVICE: THERIFIL BONE FILLER
THERICS, INC.                     510(k) NO: K031040(TRADITIONAL)
ATTN: UMBERTO V PARROTTA, JR      PHONE NO : 609-501-7200
115 CAMPUS DR.                    SE DECISION MADE: 24-JUL-03
PRINCETON, NJ 08540               510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: SPI DENTAL IMPLANT ABUTMENTS
THOMMEN MEDICAL, AG               510(k) NO: K031747(SPECIAL)
ATTN: FLOYD G LARSON              PHONE NO : 858-792-1235
4329 GRAYDON RD.                  SE DECISION MADE: 02-JUL-03
SAN DIEGO, CA 92130               510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: THYRO TEST
THRYOTEC                          510(k) NO: K030912(TRADITIONAL)
ATTN: FRAN  WHITE                 PHONE NO : 978-927-3808
163 CABOT STREET                  SE DECISION MADE: 25-JUL-03
BEVERLY, MA 01915                 510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: TINNITUS RX
TINNITUS CONTROL, INC.            510(k) NO: K031624(TRADITIONAL)
ATTN: RUSS  PAGANO                PHONE NO : 202-546-1262
719 A STREET, NE                  SE DECISION MADE: 24-JUL-03
WASHINGTON, DC 20002              510(k) SUMMARY AVAILABLE FROM FDA

 
DEVICE: CROSSPOINT TRANSACCESS CATHETER, MODEL TA-XP-001
TRANS VASCULAR INCORPORATED       510(k) NO: K031920(SPECIAL)
ATTN: RICHARD E ANDERSON          PHONE NO : 650-473-4500
1505-D ADAMS DR.                  SE DECISION MADE: 23-JUL-03
MENLO PARK, CA 94925              510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: SENSITITRE 18-24 HOUR SUSCEPTIBILITY PLATE
TREK DIAGNOSTIC SYSTEMS, INC.     510(k) NO: K031545(TRADITIONAL)
ATTN: CYNTHIA C KNAPP             PHONE NO : 216-351-8735
982 KEYNOTE CIRCLE SUITE 6        SE DECISION MADE: 16-JUL-03
CLEVELAND, OH 44131               510(k) STATEMENT

DEVICE: MODIFICATION TO WBR, MODEL HR
U.C.G. TECHNOLOGIES LTD.          510(k) NO: K031874(SPECIAL)
ATTN: DAN  LAOR                   PHONE NO : 972 4 8546611
BUILDING # 30 MATAM               SE DECISION MADE: 18-JUL-03
HAIFA, ISRAEL 31905               510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: PRIMA III TOTALSENSE TORSO COIL
USA INSTRUMENTS, INC.             510(k) NO: K031365(TRADITIONAL)
ATTN: CHRISTIE  SHUMAKER          PHONE NO : 330-562-1000
1515 DANNER DR.                   SE DECISION MADE: 18-JUL-03
AURORA, OH 44202                  510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: PREMIER 9000 8 CHANNEL PHASED ARRAY CTL SPINE COIL
USA INSTRUMENTS, INC.             510(k) NO: K031366(TRADITIONAL)
ATTN: CHRISTIE  SHUMAKER          PHONE NO : 330-562-1000
1515 DANNER DR.                   SE DECISION MADE: 11-JUL-03
AURORA, OH 44202                  510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: BUTLER GUM PROPHY PASTE WITH NOVAMIN
USBIOMATERIALS CORP.              510(k) NO: K024343(TRADITIONAL)
ATTN: DAVID C GREENSPAN           PHONE NO : 386-418-1551
13709 PROGRESS BLVD.              SE DECISION MADE: 11-JUL-03
#23                               510(k) SUMMARY AVAILABLE FROM FDA
ALACHUA, FL 32615

DEVICE: VASC-ALERT
VASC-ALERT L.L.C.                 510(k) NO: K030456(TRADITIONAL)
ATTN: JOHN  KENNEDY               PHONE NO : 773-334-8177
1807 W. SUNNYSIDE AVE.            SE DECISION MADE: 11-JUL-03
SUITE 301                         510(k) SUMMARY AVAILABLE FROM FDA
CHICAGO, IL 60640

DEVICE: VENTLAB BACTERIAL FILTER, MODEL BF100
VENTLAB CORP.                     510(k) NO: K030271(TRADITIONAL)
ATTN: ROBERT M KELLY              PHONE NO : 336-492-2636
2934 HWY. 601 NORTH               SE DECISION MADE: 07-JUL-03
MOCKSVILLE, NC 27028              510(k) STATEMENT

DEVICE: SPIROSOFT
VIASYS HEALTHCARE GMBH            510(k) NO: K031194(SPECIAL)
ATTN: EARL  DRAPER                PHONE NO : 714-283-2228
22705 SAVI RANCH PKWY.            SE DECISION MADE: 30-JUL-03
YORBA LINDA, CA 92887             510(k) STATEMENT

 
DEVICE: ENDOS DC
VILLA SISTEMI MEDICALI S.P.A.     510(k) NO: K030634(ABBREVIATED)
ATTN: ANDREW  HRYNDZA             PHONE NO : 847-288-7000
11550 WEST KING ST.               SE DECISION MADE: 21-JUL-03
FRANKLIN PARK, IL 60131           510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: RSV (RADIOLOGY SYSTEM VISIODENT
VISIODENT SA                      510(k) NO: K031448(TRADITIONAL)
ATTN: CLAUDE D BERTHOIN           PHONE NO : 386-672-0450
110 E GRANADA BLVD.               SE DECISION MADE: 31-JUL-03
STE 207 & 208; PO BOX 36          510(k) STATEMENT
ORMOND BEACH, FL 32175-0036

DEVICE: SLIDE-ON ENDOSHEATH SYSTEM FOR SENSORY TESTING
VISION-SCIENCES, INC.             510(k) NO: K031790(TRADITIONAL)
ATTN: PAMELA  PAPINEAU            PHONE NO : 978-772-3552
5 WHITCOMB AVE.                   SE DECISION MADE: 02-JUL-03
AYER, MA 01432                    510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: REUSABLE MULTIPLE-PATIENT LIFESHIRT WITH VIVOLOGIC ANALYSIS SOFT
VIVOMETRICS, INC.                 510(k) NO: K031550(TRADITIONAL)
ATTN: HOWARD M HOLSTEIN           PHONE NO : 202-637-5813
555 THIRTEENTH ST. NW             SE DECISION MADE: 29-JUL-03
WASHINGTON, DC 20004-1109         510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: UNIT, CAUTERY, TEHRMAL,BATTERY-POWERED
WALSH MEDICAL DEVICES, INC.       510(k) NO: K030158(TRADITIONAL)
ATTN: DAVID  STILES               PHONE NO : 905 844 8344
1200 SOUTH SERVICE RD. WEST       SE DECISION MADE: 17-JUL-03
UNIT 3                            510(k) SUMMARY AVAILABLE FROM FDA
OAKVILLE, ONTARIO, CANADA L6L 5T7

DEVICE: BODY SIGNAL ECG ELECTRODE
WANDY RUBBER INDUSTRIAL CO., LTD  510(k) NO: K031174(TRADITIONAL)
ATTN: JANIS  YANG                 PHONE NO : 886 2 26943185
NO.24, ALLEY 37, LANE 392         SE DECISION MADE: 10-JUL-03
FU TEH 1ST RD.                    510(k) STATEMENT
SHI-CHIH, CHINA (TAIWAN) 221

DEVICE: COACH 888
WHEELCHAIR & SCOOTER EXPRESS      510(k) NO: K030758(TRADITIONAL)
ATTN: CHRIS  TINSLEY              PHONE NO : 620-325-2629
4905 A. SAN JACINTO               SE DECISION MADE: 31-JUL-03
HOUSTON, TX 77004                 510(k) STATEMENT

DEVICE: COACH 888W
WHEELCHAIR & SCOOTER EXPRESS      510(k) NO: K030760(TRADITIONAL)
ATTN: CHRIS  TINSLEY              PHONE NO : 620-325-2629
4905 A. SAN JACINTO               SE DECISION MADE: 10-JUL-03
HOUSTON, TX 77004                 510(k) STATEMENT

DEVICE: 5MP TFT LCD MONITOR SYSTEM IF2105A BY WIDE CORPORATION
WIDE CORPORATION                  510(k) NO: K031929(TRADITIONAL)
ATTN: CARL  ALLETTO               PHONE NO : 940-300-8601
1100 LAKEVIEW BLVD.               SE DECISION MADE: 08-JUL-03
DENTON, TX 76208                  510(k) SUMMARY AVAILABLE FROM FDA
                                  THIRD PARTY REVIEW

 
DEVICE: WIDE 3MP GRAYSCALE TFT LCD MONITOR IF2103A
WIDE CORPORATION                  510(k) NO: K032174(TRADITIONAL)
ATTN: CARL  ALLETTO               PHONE NO : 940-300-8601
1100 LAKEVIEW BLVD.               SE DECISION MADE: 24-JUL-03
DENTON, TX 76208                  510(k) SUMMARY AVAILABLE FROM FDA
                                  THIRD PARTY REVIEW

DEVICE: READI-STRAND, MODEL PSSTRAND
WORLDWIDE MEDICAL TECHNOLOGIES, IN510(k) NO: K023179(TRADITIONAL)
ATTN: GARY  LAMOUREUX             PHONE NO : 203-263-2579
426 MAIN ST. NORTH                SE DECISION MADE: 02-JUL-03
WOODBURY, CT 06798-0505           510(k) STATEMENT

DEVICE: CELLPLEX TCP SYNTHETIC CANCELLOUS BONE
WRIGHT MEDICAL TECHNOLOGY, INC.   510(k) NO: K031817(SPECIAL)
ATTN: EHAB M ESMAIL               PHONE NO : 901-867-4732
5677 AIRLINE RD.                  SE DECISION MADE: 17-JUL-03
ARLINGTON, TN 38002               510(k) SUMMARY AVAILABLE FROM FDA

DEVICE: ENTERALITE INFINITY ENTERAL FEEDING PUMP
ZEVEX INTL., INC.                 510(k) NO: K031199(TRADITIONAL)
ATTN: SEAN M CURRY                PHONE NO : 858-675-8200
16787 BERNARDO CENTER DR.         SE DECISION MADE: 09-JUL-03
SUITE A-1                         510(k) SUMMARY AVAILABLE FROM FDA
SAN DIEGO, CA 92128


 
                                                TOTAL 510(k)s THIS PERIOD   300
                                                TOTAL WITH SUMMARIES        243
                                                TOTAL WITH STATEMENTS        57
    
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