Medical Device Recalls
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1 result found
510(K) Number: K833762 |
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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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| Percutaneous Entry Set, Nephrostomy Catheter, Global Product No. G14649 | 2 | 02/04/2020 | Cook Inc. |
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