Medical Device Recalls
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1 result found
510(K) Number: K160570 |
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Product Description
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Recall
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FDA Recall
Posting Date |
Recalling Firm
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| Creatine Kinase (CK) used on cobas c 311/501/502 and COBAS INTEGRA 400 plus-In vitro test for the qu... | 2 | 09/20/2024 |
FEI # 1823260 Roche Diagnostics Operations, Inc. |
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