Dockets:

Dockets Management

2006N-0292
BKG 2
Volume 2

Reference 1 - Letter from Pete Sessions, Mike Doyle, Tim Murphy, Michael Conaway, Bill Jenkins, Bob Inglis, George Radarovich, Members of Congress to Lester M. Crawford, Acting Commissioner, Food and Drug Administration, dated May 24, 2005.

Reference 2 - Letter from Margaret Reagan (Premiere, Inc.), Rick Pollack (American Hospital Association), Larry Gage (National Association of Public Hospitals and Health Systems), Charles Kahn (Federation of American Hospitals), Edward Goodman (Veterans Health Administration), Michael Rodgers (Catholic Health Association of the United States), Robert Dickler (Association of American Medical Colleges) to Lester Crawford, Acting Commissioner, Food and Drug Administration, dated May 9, 2005.

Reference 3 - The Food and Drug Law Institute/CDRH Report on Meeting to Discuss Unique Device Identification, (http://www.fda.gov/cdrh/ocd/uidevices061405.html), April 14 and 15, 2005.

Reference 4 - ECRI/FDA White Paper: Automatic Identification of Medical Devices, (http://www.fda.gov/cdrh/ocd/ecritask4.html), August 17, 2005.

Reference 5 - The Food and Drug Law Institute/CDRH, "Report on Meeting to Discuss Unique Device Identification," (http://www.fda.gov/cdrh/ocd/uidevices011606.html), October 27, 2005.

Reference 6 - "ERG Final Report: Unique Identification for Medical Devices," (http://www.fda.gov/cdrh/ocd/udi/erg-report.html), March 22, 2006.

Reference 7 - "Ensuring the Safety of Marketed Medical Devices: CDRH's Medical Device Safety Program," (http://www.fda.gov/cdrh/postmarket/mdpi-report.pdf), January 18, 2006.

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