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U.S. Department of Health and Human Services

Medical Device Recalls
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141 to 141 of 141 Results
510(K) Number: K022947
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Terumo Advanced Perfusion System 1 base; Model 801764. NOTE: This device is not sold in the United... 2 10/31/2008 FEI # 1828100
Terumo Cardiovascular Systems Corporation
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