Medical Device Recalls
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1 result found
510(K) Number: K063787 |
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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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Hologic InPlex CF Molecular Test (IVD); Catalog Number: 95-432. | 2 | 04/27/2016 | Hologic, Inc |
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