Meridian Bioscience Announces FDA Submission for New Curian® Campy Assay
CINCINNATI, April 01, 2021 (GLOBE NEWSWIRE) -- Meridian Bioscience, Inc. (NASDAQ: VIVO) a leading global provider of diagnostic testing solutions and life science raw materials, today announced that it has made a 510(k) submission to the U.S. Food and Drug Administration (FDA) for the Companys new Curian Campy assay.
- CINCINNATI, April 01, 2021 (GLOBE NEWSWIRE) -- Meridian Bioscience, Inc. (NASDAQ: VIVO) a leading global provider of diagnostic testing solutions and life science raw materials, today announced that it has made a 510(k) submission to the U.S. Food and Drug Administration (FDA) for the Companys new Curian Campy assay.
- This assay is one of many assays in the pipeline that expands the Curian menu, continuing Meridians leadership in the gastrointestinal disease and lateral flow testing market.
- Curian Campy, for use with the Curian Analyzer, is a rapid, qualitative fluorescent immunoassay for the detection of Campylobacter spp.
- Meridian is a fully integrated life science company that develops, manufactures, markets and distributes a broad range of innovative diagnostic products.