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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 10 of 17 Results
510(K) Number: K140911
 
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DxH 600 Coulter Cellular Analysis System, Catalog No. B23858 2 01/11/2017 FEI # 2050012
Beckman Coulter Inc.
UniCel DxH 600 Coulter Cellular Analysis System, Catalog No. B23858. 2 05/24/2017 FEI # 2050012
Beckman Coulter Inc.
UniCel DxH 600 Coulter Cellular Analysis System, REF number B23858. Product Usage: Note: The DxH... 1 05/23/2019 FEI # 2050012
Beckman Coulter Inc.
UniCel DxH 600 Coulter Cellular Analysis System, Software Version 1.1.1.0, Part No. B23858 The DxH ... 2 12/16/2015 FEI # 2050012
Beckman Coulter Inc.
UniCel DxH 600 Coulter Cellular Analysis System, Software Version 3.0.2.0, Part No. 775222 The UniC... 2 12/16/2015 FEI # 2050012
Beckman Coulter Inc.
UniCel DxH 800 Coulter Cellular Analysis System, Catalog No. 629029, B24465, B24802, B68304 2 01/11/2017 FEI # 2050012
Beckman Coulter Inc.
UniCel DxH 800 Coulter Cellular Analysis System, Catalog No. 629029, B24465, B24802, B66445, B68304,... 2 05/24/2017 FEI # 2050012
Beckman Coulter Inc.
UniCel DxH 800 Coulter Cellular Analysis System, REF numbers 629029, B24465, B24802, B68304, B66445,... 1 05/23/2019 FEI # 2050012
Beckman Coulter Inc.
UniCel DxH 800 Coulter Cellular Analysis System, Software Version 3.0.2.0, Part No. 629029, B24465, ... 2 12/16/2015 FEI # 2050012
Beckman Coulter Inc.
UniCel DxH 800 and DxH 600 Coulter Cellular Analysis System. Catalog No. 629029, B24465, B24802, ... 2 09/02/2016 FEI # 2050012
Beckman Coulter Inc.
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