meddevicedb.com FDA Device Reference

Ultraviolet Lamps Intended for Use in Sunlamp Products (commonly known as metal halide sunlamps)

K152095 Class II Traditional
Decision Date
2015-10-28
Sponsor / Applicant
Cosmedico Light, Inc.

Technical Specification

510(k) Submission ID K152095
Product Code LEJ
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4635
Decision Date 2015-10-28
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Ultraviolet Lamps Intended for Use in Sunlamp Products (commonly known as metal halide sunlamps) received FDA 510(k) clearance under submission number K152095, sponsored by Cosmedico Light, Inc.. 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 2015-10-28.

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.