Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K191899 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| cobas pro integrated solutions -cobas c 503, Analyzer, chemistry (photometric discrete), for clinica... | 2 | 12/29/2020 |
FEI # 1823260 Roche Diagnostics Operations, Inc. |
| Roche cobas pro integrated solutions (cobas pro ISE, cobas c 503, and cobas e 801 analytical units) ... | 2 | 12/30/2020 |
FEI # 1823260 Roche Diagnostics Operations, Inc. |
| cobas pro integrated solutions with cobas c 503 analytical units: cobas pro sample supply unit, m... | 2 | 02/27/2026 |
FEI # 1823260 Roche Diagnostics Operations, Inc. |
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