Medical Device Recalls
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11 to 12 of 12 Results
510(K) Number: K003565 |
Results per Page |
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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: M3841: LAERDAL brand; text prompts onl... | 2 | 11/26/2010 | Philips Medical Systems |
| Philips HeartStart FR2+ Defibrillator Automated External Defibrillator (AED) Catalog Numbers: M38... | 2 | 03/22/2007 | Philips Medical Systems |
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