meddevicedb.com FDA Device Reference

Various Brands of Ultraviolet Lamps

K150778 Class II Traditional
Decision Date
2015-05-29
Sponsor / Applicant
Cosmedico Light, Inc.

Technical Specification

510(k) Submission ID K150778
Product Code LEJ
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4635
Decision Date 2015-05-29
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Various Brands of Ultraviolet Lamps received FDA 510(k) clearance under submission number K150778, 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 2015-05-29.

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.