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# FDA Clears Meridian Campylobacter Assay
- URL: https://www.fdaweb.com/fda-clears-meridian-campylobacter-assay/
- Published: 2022-01-05T12:00:00.000Z
- Updated: 2026-09-14T17:27:35.000Z
- Author: David McFarland
- Tags: Devices, #legacy-id-D5150873

FDA has cleared a Meridian Bioscience 510(k) for the Curian Campy assay, a rapid, qualitative fluorescent immunoassay for detecting *Campylobacter*\-specific antigen including *C. jejuni*, *C. coli*, *C. upsaliensis*, and *C. lari* in human fecal specimens. It produces objective results in about 20 minutes on the company’s Curian testing platform, according to Meridian. In 3/2020, the agency cleared a 510(k) for Meridian’s Curian HpSA assay detecting *Helicobacter pylori* antigens in human stool for use on the testing platform.