Medical Device Recalls
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1 result found
510(K) Number: K010257 |
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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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| Zoll M Series Automated Defibrillator (AED) | 2 | 09/17/2004 |
FEI # 1220908 Zoll Medical Corporation |
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