meddevicedb.com FDA Device Reference

V-CLASSIC

K911535 Class II Traditional
Decision Date
1991-04-29
Sponsor / Applicant
Metalor Dental USA Corp.

Technical Specification

510(k) Submission ID K911535
Product Code EJT
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3060
Decision Date 1991-04-29
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

V-CLASSIC received FDA 510(k) clearance under submission number K911535, sponsored by Metalor Dental USA Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 1991-04-29.

Classification & Regulation

This clearance is catalogued under FDA product code EJT and 21 CFR 872.3060, within the Dental review panel as a Class II device.