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MODEL G-61 ULTRASONIC DENTAL UNIT

K791585 Class II Traditional
Decision Date
1979-09-19
Sponsor / Applicant
Cavitron Corp.

Technical Specification

510(k) Submission ID K791585
Product Code ELC
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.4850
Decision Date 1979-09-19
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MODEL G-61 ULTRASONIC DENTAL UNIT received FDA 510(k) clearance under submission number K791585, sponsored by Cavitron 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 1979-09-19.

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.