PCH

Gastrointestinal Pathogen Panel Multiplex Nucleic Acid-Based Assay System

Product code

PCH

Device name

Gastrointestinal Pathogen Panel Multiplex Nucleic Acid-Based Assay System

Device class

Class 2

21 CFR

21 CFR 866.3990

Medical specialty

Microbiology

Marketing pathway

510(K)

510(k) clearances (last 3 years)

13

Summaries archived here

13 (direct download)

510(k) clearances (all years, FDA)

38 (all years; only the last 3 years are listed here)

FDA classification definition

A gastrointestinal pathogen panel multiplex nucleic acid assay is a qualitative in vitro diagnostic device intended to simultaneously detect and identify multiple gastrointestinal microbial nucleic acids extracted from human stool specimens. The detection and identification of a specific gastrointestinal microbial nucleic acid from individuals exhibiting signs and/or symptoms of gastrointestinal infection aids in the diagnosis of gastrointestinal infection when used in conjunction with clinical evaluation and other laboratory findings.

Definition text from the FDA device classification database (U.S. federal government work, public domain).

510(k) clearances, last 3 years (13)

Last three years. Most recent: 2026-05-19.

13 summaries are archived here for direct download.