Medical Device Recalls
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1 result found
510(K) Number: K980759 |
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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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| Product is labeled in part: "***is immunosimplicity***ENA-6 Screen***Enzyme Immunoassay Test Kit***... | 2 | 05/21/2012 |
FEI # 1044713 Diamedix Corporation |
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