Medical Device Recalls
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1 result found
510(K) Number: K002262 |
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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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Product is labeled in part: "***is immunosimplicity***HSV 1&2 IgM***Enzyme Immunoassay Test Kit***F... | 3 | 05/10/2012 | Diamedix Corporation |
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