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U.S. Department of Health and Human Services

Medical Device Recalls
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11 to 20 of 25 Results
510(K) Number: K040438
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FDA Recall
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Cardio Vive 92532 AED, BURDICK Manufactured by Cardiac Science Corporation, Automated External Defi... 2 02/25/2009 Cardiac Science Corporation
Cardiovive 92532 automated external defibrillator. This semi-automatic model requires the user to... 2 04/06/2010 Cardiac Science Corporation
GE Responder 2019198 automated external defibrillator. This semi-automatic model requires the user ... 1 03/04/2010 Cardiac Science Corporation
GE Responder 2023440 automated external defibrillator. This semi-automatic model requires the user ... 1 03/04/2010 Cardiac Science Corporation
NK 9200G. CardioLife automated external defibrillator. This semi-automatic model requires the user ... 1 03/04/2010 Cardiac Science Corporation
NK 9231 CardioLife automated external defibrillator. This semi-automatic model requires the user to... 1 03/04/2010 Cardiac Science Corporation
Powerheart 9300A automated external defibrillator. This fully automatic model does not require the ... 2 04/06/2010 Cardiac Science Corporation
Powerheart 9300E automated external defibrillator. This semi-automatic model requires the user to... 2 04/06/2010 Cardiac Science Corporation
Powerheart 9300P automated external defibrillator. This semi-automatic model requires the user to... 2 04/06/2010 Cardiac Science Corporation
Powerheart 9390A automated external defibrillator. This fully automatic model does not require th... 2 04/06/2010 Cardiac Science Corporation
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