Medical Device Recalls
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1 result found
510(K) Number: K112945 |
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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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EliteCore Full Core Biopsy Device. EliteCore 18G, 20cm with and without HiLiter tip, 15 cm with and... | 2 | 05/26/2015 | Stryker Instruments Div. of Stryker Corporation |
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