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U.S. Department of Health and Human Services

Medical Device Recalls
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510(K) Number: K991274
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Diamedix Is-Mumps IgG Enzyme Immunoassay Test Kit for In Vitro Diagnostic Use Catalog No. 720-540 3 07/28/2018 FEI # 1044713
Diamedix Corporation
Diamedix Is-Mumps IgG Test Kit Diamedix Is-Mumps IgG Test Kit is an EIA procedure intended for t... 2 05/16/2016 FEI # 1044713
Diamedix Corporation
The ETI-Mumps IgG Enzyme Immunoassay Test Kit is sold with assay software version 1.0. that is desig... 2 02/23/2006 FEI # 2182595
Diasorin Inc.
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