Medical Device Recalls
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1 result found
510(K) Number: K983196 |
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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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adult defibrillation, cardioversion, pacing, monitoring Disposable Electrodes, Model P-211-M1 and P-... | 2 | 05/30/2013 | TZ Medical Inc. |
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