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PIEZON ULTRASONIC SCALER

K821810 Class II Traditional
Decision Date
1982-07-06
Sponsor / Applicant
Healthco, Inc.

Technical Specification

510(k) Submission ID K821810
Product Code ELC
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.4850
Decision Date 1982-07-06
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PIEZON ULTRASONIC SCALER received FDA 510(k) clearance under submission number K821810, sponsored by Healthco, 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 1982-07-06.

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.