Medical Device Recalls
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1 result found
510(K) Number: K781978 |
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Product Description
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Recall
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FDA Recall
Posting Date |
Recalling Firm
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| Description/REF: CVC KIT: 16 GA X 8IN/AK-04210, CVC KIT: 1-L 16 GA X 8IN (20 CM)/AK-04300, CVC KIT: ... | 1 | 06/13/2026 |
FEI # 3013162291 ARROW INTERNATIONAL, LLC |
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