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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 6 of 6 Results
510(K) Number: K972608
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Liquid Assayed Specific Protein Control Level 2- In vitro diagnostic use, in the quality control of... 2 01/05/2023 Randox Laboratories Ltd.
Liquid Assayed Specific Protein- In vitro diagnostic use, in the quality control of serum on clinica... 2 01/05/2023 Randox Laboratories Ltd.
Liquid Assayed Specific Protein Control Level 3- In vitro diagnostic use, in the quality control of ... 2 01/05/2023 Randox Laboratories Ltd.
Randox Liquid Assayed Specific Protein Control - Level 2 (SP Control 2), Cat. no. PS2683 2 06/13/2018 Randox Laboratories Ltd.
Randox Liquid Assayed Specific Protein Control - Level 1 (SP Control 1), Cat. no. PS2682 2 06/13/2018 Randox Laboratories Ltd.
Randox Liquid Assayed Specific Protein Control - Level 3 (SP Control 3), Cat. no. PS2684 2 06/13/2018 Randox Laboratories Ltd.
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