meddevicedb.com FDA Device Reference

BEAUTISEALANT

K111782 Class II Traditional
Decision Date
2011-09-16
Sponsor / Applicant
Shofu Dental Corporation

Technical Specification

510(k) Submission ID K111782
Product Code EBC
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3765
Decision Date 2011-09-16
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BEAUTISEALANT received FDA 510(k) clearance under submission number K111782, 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 2011-09-16.

Classification & Regulation

This clearance is catalogued under FDA product code EBC and 21 CFR 872.3765, within the Dental review panel as a Class II device.