meddevicedb.com FDA Device Reference

Clear21

K192202 Class II Traditional
Decision Date
2019-11-12
Sponsor / Applicant
World Class Technology Corporation

Technical Specification

510(k) Submission ID K192202
Product Code NJM
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.5470
Decision Date 2019-11-12
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Clear21 received FDA 510(k) clearance under submission number K192202, sponsored by World Class Technology Corporation. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2019-11-12.

Classification & Regulation

This clearance is catalogued under FDA product code NJM and 21 CFR 872.5470, within the Dental review panel as a Class II device.