meddevicedb.com FDA Device Reference

Clinpro Varnish

K151302 Class II Traditional
Decision Date
2015-09-18
Sponsor / Applicant
3M Company

Technical Specification

510(k) Submission ID K151302
Product Code LBH
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3260
Decision Date 2015-09-18
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Clinpro Varnish received FDA 510(k) clearance under submission number K151302, sponsored by 3M Company. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2015-09-18.

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.