meddevicedb.com FDA Device Reference

THERALIGHT UV120-2 UVA/UVB PHOTOTHERAPY SYSTEM

K024020 Class II Traditional
Decision Date
2003-01-17
Sponsor / Applicant
Theralight, Inc.

Technical Specification

510(k) Submission ID K024020
Product Code FTC
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4630
Decision Date 2003-01-17
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

THERALIGHT UV120-2 UVA/UVB PHOTOTHERAPY SYSTEM received FDA 510(k) clearance under submission number K024020, sponsored by Theralight, 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 2003-01-17.

Classification & Regulation

This clearance is catalogued under FDA product code FTC and 21 CFR 878.4630, within the General, Plastic Surgery review panel as a Class II device.