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MAXISONIC FAMILY AND SWIFT ULTRASONIC SCALER

K051910 Class II Traditional
Decision Date
2005-09-02
Sponsor / Applicant
D.B.I. America Corp.

Technical Specification

510(k) Submission ID K051910
Product Code ELC
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.4850
Decision Date 2005-09-02
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MAXISONIC FAMILY AND SWIFT ULTRASONIC SCALER received FDA 510(k) clearance under submission number K051910, sponsored by D.B.I. America 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 2005-09-02.

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.