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FACEMASTER FACIAL TONING SYSTEM

K040871 Class II Traditional
Decision Date
2005-06-01
Sponsor / Applicant
Facemaster of Beverly Hills, Inc.

Technical Specification

510(k) Submission ID K040871
Product Code NFO
Medical Specialty / Panel Neurology
Regulation Citation 21 CFR 882.5890
Decision Date 2005-06-01
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

FACEMASTER FACIAL TONING SYSTEM received FDA 510(k) clearance under submission number K040871, sponsored by Facemaster of Beverly Hills, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Neurology review panel. The statutory decision date of record is 2005-06-01.

Classification & Regulation

This clearance is catalogued under FDA product code NFO and 21 CFR 882.5890, within the Neurology review panel as a Class II device.