meddevicedb.com FDA Device Reference

BESTALOY

K033434 Class II Traditional
Decision Date
2003-11-12
Sponsor / Applicant
We Dong Myung Dental Industrial Co., Ltd.

Technical Specification

510(k) Submission ID K033434
Product Code EJJ
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3070
Decision Date 2003-11-12
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BESTALOY received FDA 510(k) clearance under submission number K033434, sponsored by We Dong Myung Dental Industrial Co., Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2003-11-12.

Classification & Regulation

This clearance is catalogued under FDA product code EJJ and 21 CFR 872.3070, within the Dental review panel as a Class II device.