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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: K942458
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Human Assayed Multi-Sera Level 2, Model NO. HN1530 Product Usage: This product is intended for i... 2 08/06/2019 Randox Laboratories, Limited
MedTest DX Assayed Human Multi Sera Control Level 1 (HNC200) and Level 2 (HEC200) HEC200 " Sml a... 3 06/08/2017 Medtest Holdings, Inc.
MedTest DX Control Reconstitution Fluid Kit configuration: 20 x 5 ml. Bottle: 5 ml amber glass ... 2 09/15/2015 MedtestDx, Inc.
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