Medical Device Recalls
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1 result found
510(K) Number: K974552 |
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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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| Measles IgG Enzyme Immunoassay Test Kit, DIAMEDIX. The assay is intended for the semi-quantitation ... | 2 | 01/07/2009 |
FEI # 1044713 Diamedix Corporation |
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