Medical Device Recalls
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1 result found
510(K) Number: K811276 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Pruitt Occlusion Catheter. Catalog Numbers: 2103-36, 2103-46, 2103-56, E2103-36, E2103-46, E2103-56 | 2 | 05/12/2025 | LeMaitre Vascular, Inc. |
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