meddevicedb.com FDA Device Reference

LG BEAUTY LED MASK

K170984 Class II Traditional
Decision Date
2017-08-23
Sponsor / Applicant
Lg Electronics

Technical Specification

510(k) Submission ID K170984
Product Code OHS
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4810
Decision Date 2017-08-23
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

LG BEAUTY LED MASK received FDA 510(k) clearance under submission number K170984, sponsored by Lg Electronics. The device was reviewed via the Traditional premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 2017-08-23.

Classification & Regulation

This clearance is catalogued under FDA product code OHS and 21 CFR 878.4810, within the General, Plastic Surgery review panel as a Class II device.