Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K163569 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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cobas e 801 immunoassay analyzer | 2 | 05/02/2019 | Roche Diagnostics Corporation |
cobas e 801 immunoassay analyzer, cobas 8000 Modular Series The device is a fully automated, soft... | 2 | 06/10/2018 | Roche Diagnostics Corporation |
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