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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 10 of 25 Results
510(K) Number: K040438
 
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Product Description
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FDA Recall
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Burdick Cardiovive 92531 automated external defibrillator. This semi-automatic model requires the u... 1 03/04/2010 Cardiac Science Corporation
Burdick Cardiovive 92532 automated external defibrillator. This semi-automatic model requires the u... 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
Cardiac Science Powerheart 9300P automated external defibrillator. This semi-automatic model requ... 1 03/04/2010 Cardiac Science Corporation
Cardiac Science Powerheart 9300A automated external defibrillator. This fully automatic model does ... 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
Cardiac Science Powerheart 9300D automated external defibrillator. This semi-automatic model requir... 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 9390A automated external defibrillator. This fully automatic model does ... 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
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