meddevicedb.com FDA Device Reference

E-Z Chek Chlorine Residual Test Strips (K100-0101B)

K222167 Class II Traditional
Decision Date
2022-10-18
Sponsor / Applicant
Reprocessing Products Corporation (Rpc)

Technical Specification

510(k) Submission ID K222167
Product Code MSY
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5665
Decision Date 2022-10-18
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

E-Z Chek Chlorine Residual Test Strips (K100-0101B) received FDA 510(k) clearance under submission number K222167, sponsored by Reprocessing Products Corporation (Rpc). The device was reviewed via the Traditional premarket notification pathway and assigned to the Gastroenterology, Urology review panel. The statutory decision date of record is 2022-10-18.

Classification & Regulation

This clearance is catalogued under FDA product code MSY and 21 CFR 876.5665, within the Gastroenterology, Urology review panel as a Class II device.