meddevicedb.com FDA Device Reference

MAJOR QUALITY GLUCOSE AND KETONES URINE TEST

K870500 Class II Traditional
Decision Date
1987-03-06
Sponsor / Applicant
American Diagnostic Corp.

Technical Specification

510(k) Submission ID K870500
Product Code JIL
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1340
Decision Date 1987-03-06
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MAJOR QUALITY GLUCOSE AND KETONES URINE TEST received FDA 510(k) clearance under submission number K870500, sponsored by American Diagnostic Corp.. 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 1987-03-06.

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.