meddevicedb.com FDA Device Reference

ILLUMASK ACNE LIGHT THERAPY MASK

K123999 Class II Traditional
Decision Date
2013-08-28
Sponsor / Applicant
La Lumiere, LLC

Technical Specification

510(k) Submission ID K123999
Product Code OLP
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4810
Decision Date 2013-08-28
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ILLUMASK ACNE LIGHT THERAPY MASK received FDA 510(k) clearance under submission number K123999, sponsored by La Lumiere, LLC. 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 2013-08-28.

Classification & Regulation

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