Medical Device Recalls
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1 result found
510(K) Number: K172567 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Gore Molding & Occlusion Balloon Catheter, REF Catalogue Number MOB37, SN XXXXXXXX, 10 mm - 37 m 10 ... | 2 | 08/25/2021 |
FEI # 3007284313 W. L. Gore & Associates Inc. |
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