Medical Device Recalls
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1 result found
510(K) Number: K221902 |
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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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| Brand Name: LimFlow Vector Product Name: LimFlow Vector Model/Catalog Number: VT-US-23 | 2 | 01/29/2026 |
FEI # 3023527320 LimFlow, Inc. |
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