Medical Device Recalls
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1 result found
510(K) Number: K941536 |
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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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| Mechanical Filter with Connector Small, Tethered Cap, Item Code 351/5979 - Product Usage: indicated ... | 2 | 06/16/2021 |
FEI # 1219930 Covidien, LP |
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