Medical Device Recalls
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1 result found
510(K) Number: K223210 |
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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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| ClotTriever XL Catheter, 30 mm, REF: 41-102, used with Instructions for Use ClotTriever XL Cathete... | 1 | 08/21/2024 |
FEI # 3020347218 Inari Medical - Oak Canyon |
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