meddevicedb.com FDA Device Reference

ELECTRO-LIGHT THERAPY

K090250 Class II Traditional
Decision Date
2010-02-11
Sponsor / Applicant
Hill Laboratories Co.

Technical Specification

510(k) Submission ID K090250
Product Code ILY
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.5500
Decision Date 2010-02-11
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ELECTRO-LIGHT THERAPY received FDA 510(k) clearance under submission number K090250, sponsored by Hill Laboratories Co.. 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 2010-02-11.

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.