Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K162076 |
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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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PPM CLINICAL CHROMID MRSA S AUREUS 20PLT US, CATALOG 414524 | 2 | 01/04/2023 | Biomerieux Inc |
PPM CLINICAL CHROMID MRSA 20 PLT US, CATALOG 43841 | 2 | 01/04/2023 | Biomerieux Inc |
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