Medical Device Recalls
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1 result found
510(K) Number: K131781 |
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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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| Clearview Total Uterine Manipulator (model UM750), The device is labeled in part, "ClearView(R) TOT... | 2 | 05/26/2020 | Clinical Innovations, LLC |
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