meddevicedb.com FDA Device Reference

ORAVIVE TOOTH REVITALIZING PASTE

K040473 Class II Traditional
Decision Date
2004-03-10
Sponsor / Applicant
Novamin Technology, Inc.

Technical Specification

510(k) Submission ID K040473
Product Code LBH
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3260
Decision Date 2004-03-10
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ORAVIVE TOOTH REVITALIZING PASTE received FDA 510(k) clearance under submission number K040473, sponsored by Novamin Technology, 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 2004-03-10.

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.