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BEAUTIFIL II

K071742 Class II Traditional
Decision Date
2007-08-15
Sponsor / Applicant
Shofu Dental Corp.

Technical Specification

510(k) Submission ID K071742
Product Code EBF
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3690
Decision Date 2007-08-15
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BEAUTIFIL II received FDA 510(k) clearance under submission number K071742, sponsored by Shofu Dental Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2007-08-15.

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.