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SONX 35 ULTRASONIC BLEACHING SYSTEM; SONIWHITE ULTRA SONIC, MODEL QUICK WHITE US

K041392 Class I Traditional
Decision Date
2004-11-08
Sponsor / Applicant
CAO Group, Inc.

Technical Specification

510(k) Submission ID K041392
Product Code EEG
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.6475
Decision Date 2004-11-08
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SONX 35 ULTRASONIC BLEACHING SYSTEM; SONIWHITE ULTRA SONIC, MODEL QUICK WHITE US received FDA 510(k) clearance under submission number K041392, sponsored by CAO Group, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2004-11-08.

Classification & Regulation

This clearance is catalogued under FDA product code EEG and 21 CFR 872.6475, within the Dental review panel as a Class I device.