ClearanceBrief
510(k) K253722 ยท PCH Gastrointestinal Pathogen Panel Multiplex Nucleic Acid-Based Assay System

LIAISON PLEX Gastrointestinal Flex Assay

ApplicantLuminex Corporation, Northbrook IL, US
DecisionSubstantially Equivalent, May 19, 2026
ReceivedNov 24, 2025
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K253722

No recall in the FDA data names this 510(k).

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.