Medical Device Recalls
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1 result found
510(K) Number: K813368 |
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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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| Inrad sample master aspiration biopsy needle with hiliter sharp bevel needle, 22 ga x 2 3/8'' (6 cm)... | 2 | 02/08/2011 |
FEI # 3001237677 Inrad, Inc |
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