meddevicedb.com FDA Device Reference

BIOBEAM NARROW BAND LIGHT THERAPY DEVICES

K042813 Class II Traditional
Decision Date
2005-02-25
Sponsor / Applicant
Life Without Pain, LLC

Technical Specification

510(k) Submission ID K042813
Product Code ILY
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.5500
Decision Date 2005-02-25
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BIOBEAM NARROW BAND LIGHT THERAPY DEVICES received FDA 510(k) clearance under submission number K042813, sponsored by Life Without Pain, LLC. 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 2005-02-25.

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.