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U.S. Department of Health and Human Services

Medical Device Recalls
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510(K) Number: K102919
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Venous Hardshell Cardiotomy Reservoir, used during cardiopulmonary bypass Model ... 2 05/30/2023 FEI # 3008355164
Maquet Medical Systems USA
Venous Hardshell Cardiotomy Reservoir, used during cardiopulmonary bypass Model ... 2 05/26/2023 FEI # 3008355164
Maquet Medical Systems USA
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