Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K024098 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| cobas c 111 with ISE analyzers analyzer used in the following assays: a)Creatinine plus ver.2 Cat... | 2 | 04/10/2019 | Roche Diagnostics Corporation |
| Roche Diagnostics CREP2, Creatinine Plus Ver. 2, COBAS INTEGRA, cobas c systems, Roche Diagnostics, ... | 2 | 10/09/2008 | Roche Diagnostics Corp. |
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