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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K023763
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Fructosamine Calibrator, FR2993 This product is intended for in vitro use in the calibration of t... 2 03/15/2019 FEI # 1000361607
Randox Laboratories Ltd.
Fructosamine Control 3, FR2996 This product is intended for in vitro use in the calibration of t... 2 03/15/2019 FEI # 1000361607
Randox Laboratories Ltd.
Fructosamine Control 1, FR2994 This product is intended for in vitro use in the calibration of t... 2 03/15/2019 FEI # 1000361607
Randox Laboratories Ltd.
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