Medical Device Recalls
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1 result found
510(K) Number: K061613 |
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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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| Ventana Image Analysis System (VIAS) - PATHWAY anti-HER-2/neu (4B5) primary antibody with software v... | 2 | 03/18/2008 |
FEI # 1000125183 Ventana Medical Systems Inc |
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