meddevicedb.com FDA Device Reference

T-GEAR, MODEL TG/400-700

K993224 Class II Traditional
Decision Date
2000-02-11
Sponsor / Applicant
Dontech Products B.V.

Technical Specification

510(k) Submission ID K993224
Product Code DZB
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.5500
Decision Date 2000-02-11
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

T-GEAR, MODEL TG/400-700 received FDA 510(k) clearance under submission number K993224, sponsored by Dontech Products B.V.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2000-02-11.

Classification & Regulation

This clearance is catalogued under FDA product code DZB and 21 CFR 872.5500, within the Dental review panel as a Class II device.