meddevicedb.com FDA Device Reference

Endo Motor

K192649 Class I Traditional
Decision Date
2021-03-12
Sponsor / Applicant
Foshan Cicada Dental Instrument Co, Ltd.

Technical Specification

510(k) Submission ID K192649
Product Code EKX
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.4200
Decision Date 2021-03-12
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Endo Motor received FDA 510(k) clearance under submission number K192649, sponsored by Foshan Cicada Dental Instrument 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 2021-03-12.

Classification & Regulation

This clearance is catalogued under FDA product code EKX and 21 CFR 872.4200, within the Dental review panel as a Class I device.