meddevicedb.com FDA Device Reference

ARIES Group A Strep Assay, ARIES Group A Strep Assay Protocol File Kit

K172402 Class II Traditional
Decision Date
2017-10-30
Sponsor / Applicant
Luminex Corporation

Technical Specification

510(k) Submission ID K172402
Product Code PGX
Medical Specialty / Panel Microbiology
Regulation Citation 21 CFR 866.2680
Decision Date 2017-10-30
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ARIES Group A Strep Assay, ARIES Group A Strep Assay Protocol File Kit received FDA 510(k) clearance under submission number K172402, sponsored by Luminex Corporation. The device was reviewed via the Traditional premarket notification pathway and assigned to the Microbiology review panel. The statutory decision date of record is 2017-10-30.

Classification & Regulation

This clearance is catalogued under FDA product code PGX and 21 CFR 866.2680, within the Microbiology review panel as a Class II device.