Clearance Summary
LIAISON PLEX Gastrointestinal Flex Assay received FDA 510(k) clearance under submission number K253722, sponsored by Luminex Corporation. The device was reviewed via the Traditional premarket notification pathway and assigned to the Microbiology review panel. The statutory decision date of record is 2026-05-19.
- Submission: K253722
- Applicant / Sponsor: Luminex Corporation
- Clearance pathway: Traditional
- Review panel: Microbiology
- Device class: Class II
- Regulation citation: 21 CFR 866.3990
- Decision date: 2026-05-19
Classification & Regulation
This clearance is catalogued under FDA product code PCH and 21 CFR 866.3990, within the Microbiology review panel as a Class II device.