Medical Device Recalls
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1 result found
510(K) Number: K090987 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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The Instructions for Use (IFU) for: Gelsoft Plus Bifurcate, Gelsoft Plus Ax-Fem, GelsoftPlus ERS Ax... | 2 | 09/24/2021 | Vascutek, Ltd. |
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