meddevicedb.com FDA Device Reference

PRESIDENT The Original

K220097 Class II Traditional
Decision Date
2022-01-13
Sponsor / Applicant
Coltène/Whaledent AG

Technical Specification

510(k) Submission ID K220097
Product Code ELW
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3660
Decision Date 2022-01-13
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PRESIDENT The Original received FDA 510(k) clearance under submission number K220097, sponsored by Coltène/Whaledent AG. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2022-01-13.

Classification & Regulation

This clearance is catalogued under FDA product code ELW and 21 CFR 872.3660, within the Dental review panel as a Class II device.