Medical Device Recalls
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1 result found
510(K) Number: K992191 |
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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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DiaSorin ETI-EA-G assay kit Catalog No. 7570, lot # 113963C | 3 | 03/29/2005 | Diasorin Inc. |
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