Medical Device Recalls
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1 result found
510(K) Number: K972030 |
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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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Dryspot (R) Staphytect Plus, Catalog #DR0100M, 120 tests/kit. Latex slide agglutination test for ... | 3 | 03/20/2009 | Remel, Inc |
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