meddevicedb.com FDA Device Reference

FACIAL SPA

K122711 Class II Traditional
Decision Date
2013-09-17
Sponsor / Applicant
Nuskin

Technical Specification

510(k) Submission ID K122711
Product Code NFO
Medical Specialty / Panel Neurology
Regulation Citation 21 CFR 882.5890
Decision Date 2013-09-17
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

FACIAL SPA received FDA 510(k) clearance under submission number K122711, sponsored by Nuskin. The device was reviewed via the Traditional premarket notification pathway and assigned to the Neurology review panel. The statutory decision date of record is 2013-09-17.

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.