meddevicedb.com FDA Device Reference

LH-75 PHOTOTHERAPY SYSTEM

K091568 Class II Traditional
Decision Date
2009-11-05
Sponsor / Applicant
Lerner Medical Devices, Inc.

Technical Specification

510(k) Submission ID K091568
Product Code FTC
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4630
Decision Date 2009-11-05
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

LH-75 PHOTOTHERAPY SYSTEM received FDA 510(k) clearance under submission number K091568, sponsored by Lerner Medical Devices, 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 2009-11-05.

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.