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July 2003 Archive

FDA Public Health Web Notification: Risk of Bacterial Meningitis in Children with Cochlear Implants - Updated July 31, 2003
FDA Announces Device User Fees for FY 2004 July 31, 2003
Summary Information for - FX miniRAIL(tm) RX Percutaneous Transluminal Coronary Angioplasty PTCA Catheter - P020037 July 30, 2003
Summary Information for - ThinPrep(r) Imaging System- P020002 July 30, 2003
Summary Information for - Ceramic TRANSCEND(r) Hip Articulation System-P010001 July 30, 2003
Summary Information for - STAR S4 Active Trak(tm) Excimer Laser System and WaveScan Wave Front(r) System- P930016/S016 July 30, 2003
Summary Information for - Osteonics(r) ABC System; Trident(tm) System -P000013 July 30, 2003
Summary from the General and Plastic Surgery Devices Panel Meeting - 7/24/03 July 29, 2003
How does FCC Audit Cell Phone RF? July 29, 2003
Questions, Roster, Agenda and Briefing Material for the 7/24/03 General and Plastic Surgery Devices Panel Meeting July 21, 2003
FDA Clears New Lab Test to Help Predict Those at Risk of Coronary Heart Disease July 21, 2003
Consumer Information on: FX miniRAIL(tm) RX Percutaneous Transluminal Coronary Angioplasty PTCA Catheter July 17, 2003
Consumer Information on: FX miniRAIL(tm) RX Percutaneous Transluminal Coronary Angioplasty PTCA Catheter July 17, 2003
Consumer Information on: Dermagraft(r) July 16, 2003
Glucose Meter Test Results: Useful Tips to Increase Accuracy and Reduce Errors July 14, 2003
July-August FDA Consumer Magazine July 14, 2003
Medical Device Fellowship Program July 14, 2003
PMA Final Decisions for June 2003 July 14, 2003
User Facility Reporting Bulletin - Spring/Summer 2003 Issue July 14, 2003
Notice of Upcoming Meeting of the Neurological Devices Panel - August 5th, 2003 July 11, 2003
Summary Information for - Zenith(tm) AAA Endovascular Graft and H&L One-Shot(tm) Introduction System - P020018 July 11, 2003
Summary Information for - Dermagraft(r) -- H020004 July 9, 2003
FDA Clears First Test for West Nile Virus July 9, 2003
Medical Device Class 1 Recall: ESPRIT Ventilator - Updated July 9, 2003
OIVD Requests a Meeting with Roche Diagnostics Regarding the AmpliChip CYP450 Microarray July 8, 2003
Cordis Corporation Issues a Health Care Professional Letter Regarding the CYPHER Stent July 8, 2003
510(k)s Final Decisions Rendered for June 2003 July 8, 2003
FDA Clears New Diabetes Device for Marketing July 7, 2003
Notice of Upcoming Meeting of the Medical Devices Dispute Resolution Panel - August 20, 2003 July 7, 2003
MQSA National Statistics - Updated for July 2003 July 3, 2003
Medical Device Class 1 Recall: Espirit Ventilator (Date Recall Initiated - June 8, 2001) July 2, 2003
FDA Patient Safety News - July Edition July 1, 2003