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PIEZOMATIC ULTRASONIC SCALER (SYSTEM S)

K780808 Class II Traditional
Decision Date
1978-06-22
Sponsor / Applicant
Dental Ventures of America, Inc.

Technical Specification

510(k) Submission ID K780808
Product Code ELC
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.4850
Decision Date 1978-06-22
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PIEZOMATIC ULTRASONIC SCALER (SYSTEM S) received FDA 510(k) clearance under submission number K780808, sponsored by Dental Ventures of America, 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 1978-06-22.

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.