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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 10 of 33 Results
510(K) Number: K031987
 
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Powerheart G3 Automated External Defibrillators (Non-Wearable) and include the following models: Pow... 1 02/27/2012 FEI # 2112020
Cardiac Science Corporation
Cardiac Science, Automated External Defibrillator (AED) under the following brand names (with respec... 1 04/27/2010 FEI # 2112020
Cardiac Science Corporation
Cardiac Science Powerheart 9300E automated external defibrillator. This semi-automatic model requir... 1 03/04/2010 FEI # 2112020
Cardiac Science Corporation
Cardiac Science Powerheart 9300P automated external defibrillator. This semi-automatic model requ... 1 03/04/2010 FEI # 2112020
Cardiac Science Corporation
Cardiac Science Powerheart 9390A automated external defibrillator. This fully automatic model does ... 1 03/04/2010 FEI # 2112020
Cardiac Science Corporation
Cardiac Science Powerheart 9390E automated external defibrillator. This semi-automatic model require... 1 03/04/2010 FEI # 2112020
Cardiac Science Corporation
Burdick Cardiovive 92531 automated external defibrillator. This semi-automatic model requires the u... 1 03/04/2010 FEI # 2112020
Cardiac Science Corporation
Burdick Cardiovive 92532 automated external defibrillator. This semi-automatic model requires the u... 1 03/04/2010 FEI # 2112020
Cardiac Science Corporation
Burdick Cardiovive 92533 automated external defibrillator. This semi-automatic model requires the u... 1 03/04/2010 FEI # 2112020
Cardiac Science Corporation
GE Responder 2019198 automated external defibrillator. This semi-automatic model requires the user ... 1 03/04/2010 FEI # 2112020
Cardiac Science Corporation
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