meddevicedb.com FDA Device Reference

DREAM CLEANSE S SCALER, DREAM COMPACT S SCALER

K033044 Class II Traditional
Decision Date
2004-12-21
Sponsor / Applicant
American Green Dent. Mfg, Inc.

Technical Specification

510(k) Submission ID K033044
Product Code ELC
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.4850
Decision Date 2004-12-21
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DREAM CLEANSE S SCALER, DREAM COMPACT S SCALER received FDA 510(k) clearance under submission number K033044, sponsored by American Green Dent. Mfg, 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 2004-12-21.

Classification & Regulation

This clearance is catalogued under FDA product code ELC and 21 CFR 872.4850, within the Dental review panel as a Class II device.