meddevicedb.com FDA Device Reference

GLUTARTEST 1 REAGENT STRIP

K002011 Class II Traditional
Decision Date
2001-01-22
Sponsor / Applicant
Integrated Biomedical Technology, Inc.

Technical Specification

510(k) Submission ID K002011
Product Code MSY
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5665
Decision Date 2001-01-22
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

GLUTARTEST 1 REAGENT STRIP received FDA 510(k) clearance under submission number K002011, sponsored by Integrated Biomedical Technology, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Gastroenterology, Urology review panel. The statutory decision date of record is 2001-01-22.

Classification & Regulation

This clearance is catalogued under FDA product code MSY and 21 CFR 876.5665, within the Gastroenterology, Urology review panel as a Class II device.