meddevicedb.com FDA Device Reference

AIR SONIC SCALER

K083059 Class II Traditional
Decision Date
2009-01-30
Sponsor / Applicant
Dpm USA Corp.

Technical Specification

510(k) Submission ID K083059
Product Code ELC
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.4850
Decision Date 2009-01-30
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

AIR SONIC SCALER received FDA 510(k) clearance under submission number K083059, sponsored by Dpm USA Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2009-01-30.

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.