meddevicedb.com FDA Device Reference

QUICK CHECK 3 FILM

K903191 Class II Traditional
Decision Date
1990-10-15
Sponsor / Applicant
Quantai Biotronics, Inc.

Technical Specification

510(k) Submission ID K903191
Product Code CGA
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1345
Decision Date 1990-10-15
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

QUICK CHECK 3 FILM received FDA 510(k) clearance under submission number K903191, sponsored by Quantai Biotronics, 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 1990-10-15.

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.