Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K152245 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Online TDM Vancomycin Gen.3 ( 200 tests) Catalog # 06779344190 Analyzer/Module: cobas c 311 and co... | 2 | 10/04/2019 |
FEI # 1823260 Roche Diagnostics Operations, Inc. |
| Online TDM Vancomycin Gen.3 (100 tests) Catalog # 06779336190 Analyzer/Module: cobas c 311 and cob... | 2 | 10/04/2019 |
FEI # 1823260 Roche Diagnostics Operations, Inc. |
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