meddevicedb.com FDA Device Reference

RADIANCE PORCELAIN

K042638 Class II Traditional
Decision Date
2004-12-17
Sponsor / Applicant
Aurident, Inc.

Technical Specification

510(k) Submission ID K042638
Product Code EIH
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.6660
Decision Date 2004-12-17
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

RADIANCE PORCELAIN received FDA 510(k) clearance under submission number K042638, sponsored by Aurident, 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 2004-12-17.

Classification & Regulation

This clearance is catalogued under FDA product code EIH and 21 CFR 872.6660, within the Dental review panel as a Class II device.