Medical Device Recalls
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1 result found
510(K) Number: K123418 |
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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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AdvanDx Gram-Negative QuickFISH BC. In-Vitro Diagnostic for the identification of Enterobacteriaca... | 3 | 01/02/2014 | AdvanDx, Inc. |
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