Skip to : [Content] [Navigation]
 
More CDRH Releases

Federal Register Notices

Guidance Documents

CDRH Resources

Current FDA Warning Letter Database

Archived FDA Warning Letter Database

Releasable 510(k)s

Releasable PMAs

Releasable Establishment Registrations

Releasable Device Listings

Good Guidance Practices

More CDRH databases

More FDA Articles

Medical Device & Diagnostic Industry

In Vitro Diagnostic Technology

Pharmaceutical & Medical Packaging News

 
Other FDA Documents - Archives
February 2007 | January 2007 | December 2006 | November 2006 | October 2006 | September 2006 | August 2006 | July 2006 | June 2006 | May 2006 | April 2006 | March 2006 | February 2006 | January 2006 | December 2005 | November 2005 | October 2005 | September 2005 | August 2005 | July 2005 | June 2005 | May 2005 | April 2005 | March 2005 | February 2005 |January 2005 | December 2004 | November 2004 | October 2004 | September 2004 | August 2004 | July 2004 | June 2004 | May 2004 | April 2004 | March 2004 | February 2004 | January 2004 | December 2003 | November 2003 | October 2003 | September 2003 | August 2003 | July 2003 | June 2003 | May 2003 | April 2003 | March 2003 | February 2003 | January 2003 | December 2002 | November 2002 | October 2002 | September 2002 | August 2002 | July 2002 | June 2002 | May 2002 | April 2002 | March 2002 | February 2002 | January 2002 | December 2001 | November 2001 | October 2001 | September 2001 | July/August 2001
Other FDA Documents -March Releases
Clinical Chemistry and Clinical Toxicology Devices Panel Advisory Meeting, December 6, 2006 - Minutes
 March 29, 2007
Medical Device Safety Article: Prevent Dangerous Hemodialysis Catheter Disconnections
 March 29, 2007
Consumer Information on Breast Pumps
 March 27, 2007
Summary Information for: MESOMARK
 March 27, 2007
Consumer Information on: MESOMARK - H060004
 March 27, 2007
Class I Medical Device Recall: Smith & Nephew, Inc. Radiofrequency Denervation Probes
 March 27, 2007
11th Conference of the Global Harmonization Task Force (2007): General Announcement and Booking Information (Links to Global Harmonization Task Force Web site)
 March 26, 2007
Summary Information for: Guardian REAL-Time and Paradigm REAL-Time Systems
 March 26, 2007
Summary Information for: Stelkast Surpass Acetabular System
 March 26, 2007
Summary Information for: Therapy Cool Path Ablation Catheter and IBI 1500T9 RF Ablation Generator
 March 26, 2007
Orthopaedic and Rehabilitation Devices Panel Advisory Meeting, February 22, 2007 - Transcript
 March 22, 2007
Japan - U.S. "Harmonization By Doing" HBD Pilot Program Initiative (Updated 3/21/2007)
 March 21, 2007
Class I Medical Device Recall: HoMedics Thera-P Heating Pads
 March 19, 2007
Neurological Devices Panel Advisory Meeting, January 26, 2007 - Written Comments, Transcript
 March 19, 2007
Summary Information for: Histoacryl and Histoacryl Blue Topical Skin Adhesive
 March 16, 2007
Summary Information for: InFuse Bone Graft
 March 13, 2007
Consumer Information on: INFUSE Bone Graft - P050053
 March 13, 2007
Maturity Health Matters: FDA Health News for Older Adults and Their Caregivers (Winter 2007 Issue)
 March 13, 2007
PMA Final Decisions for February 2007
 March 9, 2007
Class I Medical Device Recall: LifeLine Semi-Automatic External Defibrillators (AEDs) and ReviveR Semi-Automatic External Defibrillators (AEDs)
 March 7, 2007
510(k) Final Decisions - February 2007
 March 5, 2007
Circulatory System Devices Panel Advisory Meeting, March 1-2, 2007 - Agenda, Roster, Questions, Briefing, Brief Summaries
 March 5, 2007
Orthopaedic and Rehabilitation Devices Panel Advisory Meeting, February 22, 2007 - Questions, Other, Slides
 March 2, 2007
Advice for Patients: Change in Daylight Savings Time May Affect Your Medical Equipment in an Unpredictable Way
 March 1, 2007
FDA Preliminary Public Health Notification: Unpredictable Events in Medical Equipment due to New Daylight Savings Time Change
March 1, 2007