meddevicedb.com FDA Device Reference

MDx-Chex for BCN

K254166 Class II Traditional
Decision Date
2026-03-23
Sponsor / Applicant
Streck

Technical Specification

510(k) Submission ID K254166
Product Code PMN
Medical Specialty / Panel Microbiology
Regulation Citation 21 CFR 866.3920
Decision Date 2026-03-23
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MDx-Chex for BCN received FDA 510(k) clearance under submission number K254166, 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 2026-03-23.

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.