Medical Device Recalls
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1 result found
510(K) Number: K791202 |
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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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| DiaSorin TRYPSIK Kits, Catalog Number P2573-(assay used as a procedure for the quantitative determin... | 3 | 04/14/2007 |
FEI # 2182595 Diasorin Inc. |
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