Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K062161 |
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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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| Gore Propaten Vascular Graft configured for Pediatric Shunt, Diameter 6 mm, Length 15 cm, Rx Only, ... | 2 | 08/13/2021 |
FEI # 2017233 W L Gore & Associates, Inc. |
| Gore Propaten Vascular Graft configured for Pediatric Shunt, Diameter 5 mm, Length 10 cm, Rx Only, ... | 2 | 08/13/2021 |
FEI # 2017233 W L Gore & Associates, Inc. |
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