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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 8 of 8 Results
510(K) Number: K040637
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Product Description
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FDA Recall
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Powerheart 9300P automated external defibrillator. This semi-automatic model requires the user to... 2 04/06/2010 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
Cardiovive 92532 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
Powerheart 9390E automated external defibrillator. This semi-automatic model requires the user to... 2 04/06/2010 Cardiac Science Corporation
Responder 2023440 automated external defibrillator. This semi-automatic model requires the user t... 2 04/06/2010 Cardiac Science Corporation
Powerheart AED G3 Automated External Defibrillator Model 9300P Professional series). Cardiac Scienc... 2 01/15/2005 Cardiac Science, Inc.
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