Medical Device Recalls
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1 result found
510(K) Number: K140465 |
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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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| uPath software 1.1 and uPath software 1.1 IVD-INSW, Material numbers 08991871001 and 09077332001 | 2 | 01/17/2021 |
FEI # 2243471 Roche Molecular Systems, Inc. |
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