meddevicedb.com FDA Device Reference

cobas Influenza A/B & RSV Nucleic acid test for use on the cobas Liat System

K210234 Class II Special
Decision Date
2021-02-16
Sponsor / Applicant
Roche Molecular Systems, Inc.

Technical Specification

510(k) Submission ID K210234
Product Code OCC
Medical Specialty / Panel Microbiology
Regulation Citation 21 CFR 866.3980
Decision Date 2021-02-16
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

cobas Influenza A/B & RSV Nucleic acid test for use on the cobas Liat System received FDA 510(k) clearance under submission number K210234, sponsored by Roche Molecular Systems, 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 2021-02-16.

Classification & Regulation

This clearance is catalogued under FDA product code OCC and 21 CFR 866.3980, within the Microbiology review panel as a Class II device.