Medical Device Recalls
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1 result found
510(K) Number: K946158 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| DiaSorin ETI-EBNA-G kits, Catalog No. P001607A. In vitro diagnostic. For the qualitative and/or ... | 3 | 04/24/2007 | Diasorin Inc. |
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