meddevicedb.com FDA Device Reference

ENAMEL PRO VARNISH

K062683 Class II Traditional
Decision Date
2006-11-21
Sponsor / Applicant
Premier Dental Products Co.

Technical Specification

510(k) Submission ID K062683
Product Code LBH
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3260
Decision Date 2006-11-21
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ENAMEL PRO VARNISH received FDA 510(k) clearance under submission number K062683, sponsored by Premier Dental Products Co.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2006-11-21.

Classification & Regulation

This clearance is catalogued under FDA product code LBH and 21 CFR 872.3260, within the Dental review panel as a Class II device.