meddevicedb.com FDA Device Reference

VISION PORCELAIN

K990790 Class II Traditional
Decision Date
1999-04-02
Sponsor / Applicant
Servo Dental USA, Inc.

Technical Specification

510(k) Submission ID K990790
Product Code EIH
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.6660
Decision Date 1999-04-02
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

VISION PORCELAIN received FDA 510(k) clearance under submission number K990790, sponsored by Servo Dental USA, 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 1999-04-02.

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.