meddevicedb.com FDA Device Reference

Tua Face Fitness / Tua Trend Face

K192077 Class II Traditional
Decision Date
2020-09-30
Sponsor / Applicant
Vupiesse S.R.L

Technical Specification

510(k) Submission ID K192077
Product Code NFO
Medical Specialty / Panel Neurology
Regulation Citation 21 CFR 882.5890
Decision Date 2020-09-30
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Tua Face Fitness / Tua Trend Face received FDA 510(k) clearance under submission number K192077, sponsored by Vupiesse S.R.L. The device was reviewed via the Traditional premarket notification pathway and assigned to the Neurology review panel. The statutory decision date of record is 2020-09-30.

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.