meddevicedb.com FDA Device Reference

KYOTEST UK URINE TEST REAGENT STRIP

K841715 Class I Traditional
Decision Date
1984-05-31
Sponsor / Applicant
Kyoto Diagnostics, Inc.

Technical Specification

510(k) Submission ID K841715
Product Code JIN
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1435
Decision Date 1984-05-31
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

KYOTEST UK URINE TEST REAGENT STRIP received FDA 510(k) clearance under submission number K841715, sponsored by Kyoto Diagnostics, 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 1984-05-31.

Classification & Regulation

This clearance is catalogued under FDA product code JIN and 21 CFR 862.1435, within the Clinical Chemistry review panel as a Class I device.