Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K014157 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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HeartStart FR2+ automated external defibrillator (AED) Model M3860: Philips brand; configurable ECG ... | 2 | 11/26/2010 | Philips Medical Systems |
HeartStart FR2+ automated external defibrillator (AED) model: M3841: LAERDAL brand; text prompts onl... | 2 | 11/26/2010 | Philips Medical Systems |
HeartStart FR2+ automated external defibrillator (AED) model: M3861: PHILIPS brand; text prompts o... | 2 | 11/26/2010 | Philips Medical Systems |
HeartStart FR2+ automated external defibrillator (AED) model: M3840: LAERDAL brand; configurable ... | 2 | 11/26/2010 | Philips Medical Systems |
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