meddevicedb.com FDA Device Reference

OPTIGLAZE COLOR

K133836 Class II Traditional
Decision Date
2014-03-06
Sponsor / Applicant
GC America, Inc.

Technical Specification

510(k) Submission ID K133836
Product Code EBD
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3310
Decision Date 2014-03-06
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

OPTIGLAZE COLOR received FDA 510(k) clearance under submission number K133836, sponsored by GC America, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2014-03-06.

Classification & Regulation

This clearance is catalogued under FDA product code EBD and 21 CFR 872.3310, within the Dental review panel as a Class II device.