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ADDITIONAL KYOTEST URINE TEST REAGENT STRIPS

K861733 Class II Traditional
Decision Date
1986-07-25
Sponsor / Applicant
Kyoto Diagnostics, Inc.

Technical Specification

510(k) Submission ID K861733
Product Code JIL
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1340
Decision Date 1986-07-25
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ADDITIONAL KYOTEST URINE TEST REAGENT STRIPS received FDA 510(k) clearance under submission number K861733, 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 1986-07-25.

Classification & Regulation

This clearance is catalogued under FDA product code JIL and 21 CFR 862.1340, within the Clinical Chemistry review panel as a Class II device.