Medical Device Recalls
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1 result found
510(K) Number: K982491 |
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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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| Calcitonin ELISA Kit, Code No. 7024, 7024BU. Intended use of this product is the quantitative det... | 2 | 12/16/2014 |
FEI # 3007981058 Biomerica |
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