Medical Device Recalls
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1 result found
510(K) Number: K924096 |
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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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Premier CMV IgG Elisa Kits, EIA diagnostic test kits, 96 tests per kit, Catalog Numbers: 620096 and ... | 2 | 08/12/2003 | Meridian Bioscience Inc |
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