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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 10 of 11 Results
510(K) Number: K060256
 
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Unicel DxC 600i System and Unicel Dxl 600 Access Immunoassay System 2 09/21/2008 FEI # 2050012
Beckman Coulter Inc
UniCel DxC 880i, 860i,680i and 660i Synchron Access Clinical Systems The Unicel DxC Integrated Wo... 2 07/11/2011 FEI # 2050012
Beckman Coulter Inc.
UniCel DxC 880i, 860i and 600i Systems; Software Part Number: A84500, A86646; Software version: 4.9... 2 09/30/2010 FEI # 2050012
Beckman Coulter Inc.
UniCel DxC 600i, Part Numbers: A25638, A25639, Beckman Coulter, Inc. 2 05/24/2008 FEI # 2050012
Beckman Coulter Inc
UniCel DxC 600i Synchron Access Clinical System; P/N 107405S Product Usage: The Access Immunoass... 2 04/01/2013 FEI # 2050012
Beckman Coulter Inc.
UniCel DxC 600i SYNCHRON Access Clinical Systems; A25656, A25638. In vitro diagnostic device used... 3 01/03/2018 FEI # 2050012
Beckman Coulter Inc.
UniCel DxC 600i SYNCHRON Access Clinical Analyzer, Catalog No. A25640, Instructions for Use Part No.... 2 11/06/2014 FEI # 2050012
Beckman Coulter Inc.
UniCel DxC 600i Access Immunoassay Systems, Part Number A25656. An in vitro diagnostic device use... 2 04/12/2011 FEI # 2050012
Beckman Coulter Inc.
Closed Tube Aliquotter (CTA) for UniCel DxC 600i, Part Number: A25637, Domestic; A25633, Internatio... 2 09/20/2010 FEI # 2050012
Beckman Coulter Inc.
Access Immunoassay Systems Assay Protocol File (APF) Software versions for UniCel DxC 600i Systems. ... 2 04/06/2012 FEI # 2050012
Beckman Coulter Inc.
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