meddevicedb.com FDA Device Reference

Bright Temporary C&B

K192830 Class II Traditional
Decision Date
2020-09-02
Sponsor / Applicant
Dmp Dental Industry S.A.

Technical Specification

510(k) Submission ID K192830
Product Code EBG
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3770
Decision Date 2020-09-02
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Bright Temporary C&B received FDA 510(k) clearance under submission number K192830, sponsored by Dmp Dental Industry S.A.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2020-09-02.

Classification & Regulation

This clearance is catalogued under FDA product code EBG and 21 CFR 872.3770, within the Dental review panel as a Class II device.