Medical Device Recalls
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1 result found
510(K) Number: K011388 |
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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 AED Plus Defibrillator (Automatic External Defibrillator) | 2 | 02/06/2003 |
FEI # 1220908 Zoll Medical Corporation |
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