meddevicedb.com FDA Device Reference

Tanning Lamp

K221523 Class II Traditional
Decision Date
2023-02-15
Sponsor / Applicant
Unilam Co., Ltd.

Technical Specification

510(k) Submission ID K221523
Product Code LEJ
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4635
Decision Date 2023-02-15
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Tanning Lamp received FDA 510(k) clearance under submission number K221523, sponsored by Unilam 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 2023-02-15.

Classification & Regulation

This clearance is catalogued under FDA product code LEJ and 21 CFR 878.4635, within the General, Plastic Surgery review panel as a Class II device.