Medical Device Recalls
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1 result found
510(K) Number: K162606 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| AssayTip/AssayCup Tray-used on the cobas e 801 module which is a part of the cobas c 8000 MODULAR An... | 2 | 10/04/2019 |
FEI # 1823260 Roche Diagnostics Operations, Inc. |
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