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URITEST 10 URINALYSIS REAGENT STRIPS

K052719 Class I Traditional
Decision Date
2006-12-05
Sponsor / Applicant
Arj Medical, Inc.

Technical Specification

510(k) Submission ID K052719
Product Code CDM
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1785
Decision Date 2006-12-05
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

URITEST 10 URINALYSIS REAGENT STRIPS received FDA 510(k) clearance under submission number K052719, sponsored by Arj Medical, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Clinical Chemistry review panel. The statutory decision date of record is 2006-12-05.

Classification & Regulation

This clearance is catalogued under FDA product code CDM and 21 CFR 862.1785, within the Clinical Chemistry review panel as a Class I device.