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xTAG Gastrointestinal Pathogen Panel (GPP), xTAG Data Analysis Software (TDAS GPP)

K183030 Class II Special
Decision Date
2018-11-30
Sponsor / Applicant
Luminex Molecular Diagnostics, Inc.

Technical Specification

510(k) Submission ID K183030
Product Code PCH
Medical Specialty / Panel Microbiology
Regulation Citation 21 CFR 866.3990
Decision Date 2018-11-30
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

xTAG Gastrointestinal Pathogen Panel (GPP), xTAG Data Analysis Software (TDAS GPP) received FDA 510(k) clearance under submission number K183030, sponsored by Luminex Molecular Diagnostics, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the Microbiology review panel. The statutory decision date of record is 2018-11-30.

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.