meddevicedb.com FDA Device Reference

Fit SA

K182869 Class II Traditional
Decision Date
2019-01-09
Sponsor / Applicant
Shofu Dental Corporation

Technical Specification

510(k) Submission ID K182869
Product Code EBF
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3690
Decision Date 2019-01-09
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Fit SA received FDA 510(k) clearance under submission number K182869, sponsored by Shofu Dental Corporation. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2019-01-09.

Classification & Regulation

This clearance is catalogued under FDA product code EBF and 21 CFR 872.3690, within the Dental review panel as a Class II device.