Medical Device Recalls
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1 result found
510(K) Number: K161217 |
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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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VITEK 2 - AST Test kits (in vitro diagnostic test cards for antimicrobial susceptibility): a) AST... | 1 | 04/25/2024 | Biomerieux Inc |
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