meddevicedb.com FDA Device Reference

ONE COAT SE BOND

K033760 Class II Traditional
Decision Date
2004-01-23
Sponsor / Applicant
Coltene/Whaledent, Inc.

Technical Specification

510(k) Submission ID K033760
Product Code KLE
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3200
Decision Date 2004-01-23
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ONE COAT SE BOND received FDA 510(k) clearance under submission number K033760, sponsored by Coltene/Whaledent, 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 2004-01-23.

Classification & Regulation

This clearance is catalogued under FDA product code KLE and 21 CFR 872.3200, within the Dental review panel as a Class II device.