Medical Device Recalls
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21 to 22 of 22 Results
510(K) Number: K063144 |
Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| VITROS 5,1 FS Chemistry System, clinical chemistry analyzer | 2 | 08/06/2019 |
FEI # 1000136573 Ortho Clinical Diagnostics |
| VITROS 5,1 FS Chemistry System, clinical chemistry analyzer | 2 | 08/06/2019 |
FEI # 1000136573 Ortho Clinical Diagnostics |
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