Medical Device Recalls
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1 result found
510(K) Number: K993435 |
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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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| Bone Marrow Aspiration Kit, consists of 3 main components packaged in a box. 1. Marrow Loc (Bone M... | 2 | 11/18/2008 |
FEI # 3002498892 Theken Spine LLC |
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