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LightStim for Pain LED Belt

K151333 Class II Traditional
Decision Date
2015-08-21
Sponsor / Applicant
Led Intellectual Properties, LLC

Technical Specification

510(k) Submission ID K151333
Product Code ILY
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.5500
Decision Date 2015-08-21
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

LightStim for Pain LED Belt received FDA 510(k) clearance under submission number K151333, sponsored by Led Intellectual Properties, 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 2015-08-21.

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.