Medical Device Recalls
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1 result found
510(K) Number: K914531 |
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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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| Arrow Arterial Kits and Trays as follows: (1) Arrow Arterial Access Tray with 0.025" Spring-Wire ... | 2 | 09/26/2024 | ARROW INTERNATIONAL Inc. |
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