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U.S. Department of Health and Human Services

Medical Device Recalls
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1 result found
510(K) Number: K790565
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Medtronic DLP Aortic Root Cannula with Flow-Guard, REF 11012; for use in cardiopulmonary bypass surg... 2 11/04/2024 FEI # 1000116158
Medtronic Perfusion Systems
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