meddevicedb.com FDA Device Reference

DUCERATIN/DUCERAM LFC DENTAL PORCELAIN

K921479 Class II Traditional
Decision Date
1992-06-22
Sponsor / Applicant
Degussa AG

Technical Specification

510(k) Submission ID K921479
Product Code EIH
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.6660
Decision Date 1992-06-22
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DUCERATIN/DUCERAM LFC DENTAL PORCELAIN received FDA 510(k) clearance under submission number K921479, sponsored by Degussa AG. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 1992-06-22.

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.