meddevicedb.com FDA Device Reference

DEL SOL RED LIGHT THERAPY SYSTEM

K072399 Class II Traditional
Decision Date
2008-05-23
Sponsor / Applicant
Edge Systems, Inc.

Technical Specification

510(k) Submission ID K072399
Product Code ILY
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.5500
Decision Date 2008-05-23
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DEL SOL RED LIGHT THERAPY SYSTEM received FDA 510(k) clearance under submission number K072399, sponsored by Edge Systems, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Physical Medicine review panel. The statutory decision date of record is 2008-05-23.

Classification & Regulation

This clearance is catalogued under FDA product code ILY and 21 CFR 890.5500, within the Physical Medicine review panel as a Class II device.