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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K102647
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ENVOY 500 AST Reagent Kit, reference Model/Catalog 55255, for Envoy 500. Intended Use of the P... 3 10/02/2014 FEI # 3007662974
ELITech Clinical Systems SAS
Viva-ProE Systems, Model # 6003-670, UDI: 03661540600357 - Product Usage: The ELITech Clinical Syst... 3 09/30/2019 FEI # 3001576181
ELITech Group B.V.
Selectra ProM Analyzer, Catalog # 6003-435/UDI # 03661540600395 and Catalog # 6003-436/UDI # 0366154... 2 10/16/2019 FEI # 2708
Vital Scientific N.V.
Selectra ProS Analyzer, Catalog # 6003-600/UDI # 03661540600418 Product Usage: :clinical chemist... 2 10/16/2019 FEI # 2708
Vital Scientific N.V.
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