meddevicedb.com FDA Device Reference

MDx-Chex for BC-GN

K231223 Class II Traditional
Decision Date
2023-07-27
Sponsor / Applicant
Streck

Technical Specification

510(k) Submission ID K231223
Product Code PMN
Medical Specialty / Panel Microbiology
Regulation Citation 21 CFR 866.3920
Decision Date 2023-07-27
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MDx-Chex for BC-GN received FDA 510(k) clearance under submission number K231223, sponsored by Streck. The device was reviewed via the Traditional premarket notification pathway and assigned to the Microbiology review panel. The statutory decision date of record is 2023-07-27.

Classification & Regulation

This clearance is catalogued under FDA product code PMN and 21 CFR 866.3920, within the Microbiology review panel as a Class II device.