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U.S. Department of Health and Human Services

Medical Device Recalls
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11 to 20 of 30 Results
510(K) Number: K081543
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VITROS 5600 Integrated System Catalog Nos. 6802413 (regular) and 6802915 (refurbished) 2 03/01/2024 FEI # 1000136573
Ortho-Clinical Diagnostics, Inc.
VITROS 5600 Integrated System Catalog Nos. 6802413 (regular) and 6802915 (refurbished) 2 03/01/2024 FEI # 1000136573
Ortho-Clinical Diagnostics, Inc.
VITROS 5600 Integrated System Product Code 6802413 and Refurbished Product Code 6802915 Running Soft... 2 12/13/2023 FEI # 1000136573
Ortho-Clinical Diagnostics, Inc.
VITROS 5600 Integrated System Software For use in the in-vitro quantitative, semi quantitative, ... 2 07/23/2012 FEI # 1000136573
Ortho-Clinical Diagnostics
VITROS 5600 Integrated System Software Version 1.6 & Below Product Usage: For use in the in vi... 2 06/01/2012 FEI # 1000305841
Ortho-Clinical Diagnostics
VITROS 5600 Integrated System, Catalog Number 6802413, Unique Device Identifier No. 10758750002740; ... 2 06/06/2016 FEI # 1000136573
Ortho-Clinical Diagnostics
VITROS 5600 Integrated System, Product Code 6802413. Intended for use in the measurement of a var... 2 04/13/2013 FEI # 1000136573
Ortho-Clinical Diagnostics
VITROS 5600 Integrated System, Product Code/Catalog Number 6802413 for in vitro diagnostic use. 2 06/09/2014 FEI # 1000136573
Ortho-Clinical Diagnostics
VITROS 5600 Integrated System, System Product Code 6802413. For use in the in vitro quantitative,... 2 10/16/2014 FEI # 1000136573
Ortho-Clinical Diagnostics
VITROS 5600 Integrated System, Unique Device Identifier No. 10758750002740 & 10758750007110. Intend... 2 04/07/2016 FEI # 1000136573
Ortho-Clinical Diagnostics
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