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U.S. Department of Health and Human Services

Medical Device Recalls
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510(K) Number: K981831
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Diamedix Is-EBV-EA-D IgG Enzyme Immunoassay Test Kit for In Vitro Diagnostic Use Catalog No. 720-640 3 07/28/2018 Diamedix Corporation
Diamedix Is-EBV-EA-D IgG Test Kit Diamedix Is-Mumps IgG Test Kit is an EIA procedure intended fo... 2 05/16/2016 Diamedix Corporation
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