meddevicedb.com FDA Device Reference

LED Light Therapy Mask (RT01)

K242068 Class II Traditional
Decision Date
2025-04-04
Sponsor / Applicant
Ningbo Dechang Electrical Machinery Made Co.,Ltd

Technical Specification

510(k) Submission ID K242068
Product Code OLP
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4810
Decision Date 2025-04-04
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

LED Light Therapy Mask (RT01) received FDA 510(k) clearance under submission number K242068, sponsored by Ningbo Dechang Electrical Machinery Made Co.,Ltd. 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 2025-04-04.

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.