meddevicedb.com FDA Device Reference

TN-Brush

K170596 Class II Traditional
Decision Date
2017-09-11
Sponsor / Applicant
Genoss Co., Ltd.

Technical Specification

510(k) Submission ID K170596
Product Code ELB
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.4840
Decision Date 2017-09-11
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TN-Brush received FDA 510(k) clearance under submission number K170596, sponsored by Genoss 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 2017-09-11.

Classification & Regulation

This clearance is catalogued under FDA product code ELB and 21 CFR 872.4840, within the Dental review panel as a Class II device.