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U.S. Department of Health and Human Services

Medical Device Recalls
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21 to 25 of 25 Results
510(K) Number: K040438
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FDA Recall
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Cardiac Science Powerheart 9300A automated external defibrillator. This fully automatic model does ... 1 03/04/2010 Cardiac Science Corporation
Burdick Cardiovive 92533 automated external defibrillator. This semi-automatic model requires the u... 1 03/04/2010 Cardiac Science Corporation
Cardio Vive 92532 AED, BURDICK Manufactured by Cardiac Science Corporation, Automated External Defi... 2 02/25/2009 Cardiac Science Corporation
Powerheart AED G3 Automated External Defibrillator Model 9300A (Automatic). Cardiac Science AEDs ar... 2 03/02/2006 Cardiac Science Corporation
Powerheart AED G3 Automated External Defibrillator Model 9300A (Automatic). Cardiac Science AEDs ar... 2 01/15/2005 Cardiac Science, Inc.
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