Medical Device Recalls
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1 result found
510(K) Number: K181354 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Stryker Neurovascular, AXS Vecta 74 Aspiration Catheter, Ref. Catalog No. INC-11597-115, Use By 2021... | 2 | 03/31/2020 |
FEI # 3008853977 Stryker Neurovascular |
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