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U.S. Department of Health and Human Services

Medical Device Recalls
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510(K) Number: K051632
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Philips, HeartStart FR2 + Defibrillator, Model # M3860A and M3861A 2 10/08/2021 FEI # 1000524572
Philips North America LLC
Heartstart FR2+ automated external defibrillator Models M3860A and M3840A are equipped with an ECG M... 2 12/08/2009 FEI # 1000524572
Philips Medical Systems
Heartstart FR2+ automated external defibrillator models M3861A and M3841A are NOT equipped with the ... 2 12/08/2009 FEI # 1000524572
Philips Medical Systems
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