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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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Product Description
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Recall
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FDA Recall
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GE Responder 2023440 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
NK 9200G. CardioLife automated external defibrillator. This semi-automatic model requires the user ... 1 03/04/2010 Cardiac Science Corporation
Burdick Cardiovive 92531 automated external defibrillator. This semi-automatic model requires the u... 1 03/04/2010 Cardiac Science Corporation
Cardiac Science Powerheart 9390E automated external defibrillator. This semi-automatic model require... 1 03/04/2010 Cardiac Science Corporation
Cardiac Science Powerheart 9390A automated external defibrillator. This fully automatic model does ... 1 03/04/2010 Cardiac Science Corporation
Cardiac Science Powerheart 9300P automated external defibrillator. This semi-automatic model requ... 1 03/04/2010 Cardiac Science Corporation
Cardiac Science Powerheart 9300E automated external defibrillator. This semi-automatic model requir... 1 03/04/2010 Cardiac Science Corporation
Cardiac Science Powerheart 9300D automated external defibrillator. This semi-automatic model requir... 1 03/04/2010 Cardiac Science Corporation
Cardiac Science Powerheart 9300C automated external defibrillator. This semi-automatic model requir... 1 03/04/2010 Cardiac Science Corporation
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