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VITA OMEGA PORCELAIN

K921474 Class II Traditional
Decision Date
1992-06-18
Sponsor / Applicant
Vident

Technical Specification

510(k) Submission ID K921474
Product Code EIH
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.6660
Decision Date 1992-06-18
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

VITA OMEGA PORCELAIN received FDA 510(k) clearance under submission number K921474, sponsored by Vident. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 1992-06-18.

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.