meddevicedb.com FDA Device Reference

BELLEGLASS HP MODELING GEL

K020178 Class II Traditional
Decision Date
2002-03-15
Sponsor / Applicant
Kerr Dental Materials Center

Technical Specification

510(k) Submission ID K020178
Product Code EBG
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3770
Decision Date 2002-03-15
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BELLEGLASS HP MODELING GEL received FDA 510(k) clearance under submission number K020178, sponsored by Kerr Dental Materials Center. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2002-03-15.

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.