meddevicedb.com FDA Device Reference

SET, TRINDER GLUCOSE

K760347 Class II Traditional
Decision Date
1976-10-05
Sponsor / Applicant
Princeton Biomedix

Technical Specification

510(k) Submission ID K760347
Product Code CGA
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1345
Decision Date 1976-10-05
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SET, TRINDER GLUCOSE received FDA 510(k) clearance under submission number K760347, sponsored by Princeton Biomedix. 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 1976-10-05.

Classification & Regulation

This clearance is catalogued under FDA product code CGA and 21 CFR 862.1345, within the Clinical Chemistry review panel as a Class II device.