meddevicedb.com FDA Device Reference

URISTIK H SERIES REAGENT STRIPS FOR URINALYSIS

K040703 Class II Traditional
Decision Date
2004-08-26
Sponsor / Applicant
Dirui Industrial Co., Ltd.

Technical Specification

510(k) Submission ID K040703
Product Code JIO
Medical Specialty / Panel Hematology
Regulation Citation 21 CFR 864.6550
Decision Date 2004-08-26
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

URISTIK H SERIES REAGENT STRIPS FOR URINALYSIS received FDA 510(k) clearance under submission number K040703, sponsored by Dirui Industrial Co., Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Hematology review panel. The statutory decision date of record is 2004-08-26.

Classification & Regulation

This clearance is catalogued under FDA product code JIO and 21 CFR 864.6550, within the Hematology review panel as a Class II device.