meddevicedb.com FDA Device Reference

BREFORMANCE

K052781 Class II Traditional
Decision Date
2005-12-09
Sponsor / Applicant
Bredent-Products For the Dental Technician Laborat

Technical Specification

510(k) Submission ID K052781
Product Code EBG
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3770
Decision Date 2005-12-09
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BREFORMANCE received FDA 510(k) clearance under submission number K052781, sponsored by Bredent-Products For the Dental Technician Laborat. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2005-12-09.

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.