meddevicedb.com FDA Device Reference

cobas liat CT/NG/MG nucleic acid test

K253759 Class II Dual Track
Decision Date
2026-05-15
Sponsor / Applicant
Roche Molecular Systems, Inc.

Technical Specification

510(k) Submission ID K253759
Product Code QEP
Medical Specialty / Panel Microbiology
Regulation Citation 21 CFR 866.3393
Decision Date 2026-05-15
Clearance Pathway Dual Track

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

cobas liat CT/NG/MG nucleic acid test received FDA 510(k) clearance under submission number K253759, sponsored by Roche Molecular Systems, Inc.. The device was reviewed via the Dual Track premarket notification pathway and assigned to the Microbiology review panel. The statutory decision date of record is 2026-05-15.

Classification & Regulation

This clearance is catalogued under FDA product code QEP and 21 CFR 866.3393, within the Microbiology review panel as a Class II device.