meddevicedb.com FDA Device Reference

ULTRASONIC SURGERY

K121620 Class II Traditional
Decision Date
2012-12-11
Sponsor / Applicant
Dmetec.Co., Ltd.

Technical Specification

510(k) Submission ID K121620
Product Code DZI
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.4120
Decision Date 2012-12-11
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ULTRASONIC SURGERY received FDA 510(k) clearance under submission number K121620, sponsored by Dmetec.Co., Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2012-12-11.

Classification & Regulation

This clearance is catalogued under FDA product code DZI and 21 CFR 872.4120, within the Dental review panel as a Class II device.