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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 10 of 141 Results
510(K) Number: K022947
 
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100/120V AC, Advanced Perfusion System 1 Product Usage: The Terumo® Advanced Perfusion System 1 ... 2 08/15/2013 FEI # 1828100
Terumo Cardiovascular Systems Corporation
100/120V AC, Advanced Perfusion System Platform (APS) The Terumo® Advanced Perfusion System 1 is ... 2 11/27/2012 FEI # 1828100
Terumo Cardiovascular Systems Corporation
100/120V AC, Advanced Perfusion System Platform (APS) The Terumo® Advanced Perfusion System 1 is ind... 2 05/28/2015 FEI # 1828100
Terumo Cardiovascular Systems Corporation
220/240V AC, Advanced Perfusion System 1 Product Usage: The Terumo® Advanced Perfusion System 1 ... 2 08/15/2013 FEI # 1828100
Terumo Cardiovascular Systems Corporation
220/240V AC, Advanced Perfusion System Platform (APS) The Terumo® Advanced Perfusion System 1 is ... 2 11/27/2012 FEI # 1828100
Terumo Cardiovascular Systems Corporation
Air bubble detect module, catalog 802110, Terumo Cardiovascular System Corp, Ann Arbor, MI. The air... 2 01/07/2011 FEI # 1828100
Terumo Cardiovascular Systems Corporation
Base for Terumo Advanced Perfusion System 1, 220/240V The Terumo® Advanced Perfusion System 1 is ind... 2 05/28/2015 FEI # 1828100
Terumo Cardiovascular Systems Corporation
Central Control Module for System 1: System 1 Base, 100/120V The Terumo Advanced Perfusion System... 2 07/06/2012 FEI # 1828100
Terumo Cardiovascular Systems Corporation
Central Control Module for System 1: System 1 Base, 220/240V The Terumo Advanced Perfusion System... 2 07/06/2012 FEI # 1828100
Terumo Cardiovascular Systems Corporation
Interface module for CDl System 100/101 Product Usage: The Interface Module for CDl 500 is the i... 2 08/21/2012 FEI # 1828100
Terumo Cardiovascular Systems Corporation
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