Medical Device Recalls
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1 result found
510(K) Number: K935457 |
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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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| Bard DuaLok Breast Lesion Localization Wire, Product Code (Gauge x Length) LW0037 (20gx37mm); LW00... | 2 | 09/16/2014 |
FEI # 2020394 Bard Peripheral Vascular Inc |
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