Medical Device Recalls
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1 result found
510(K) Number: K190779 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Trevo XP ProVue Retriever, REF (Size): 90182 (4MM x 20MM); 90185 (4MM x 30MM); 90186 (6MM x 25MM). ... | 1 | 10/21/2020 |
FEI # 3008853977 Stryker Neurovascular |
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