F.D.A. Meets With Maker of Flawed Heart Device
Wed, 25 May 2005 04:00 AM EST
By BARRY MEIER... The Food and Drug Administration and the Guidant Corporation discussed a defibrillator that has partly or totally failed in 26 cases because of an electrical flaw. ...
Related Topics
- Drug and Medical Device Safety
- Heart Disease
- Coronary Heart Disease
- Heart Defects
- Heart Murmur
- Heart Diseases
- Congestive Heart Failure
- Heart and Circulation
- Heart Attack
- Congenital Heart Disease
- Heart Bypass Surgery
- Heart Diseases--Prevention
- Coronary Disease
- Iud
- Rheumatic Disease
- Iud / Intrauterine Device
- Heart Valve Diseases
- CPAP Device
- Heart Transplantation
- Snoring

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