meddevicedb.com FDA Device Reference

LO-50 LED LIGHT SOURCE

K102167 Class II Traditional
Decision Date
2010-08-17
Sponsor / Applicant
Fiberoptics Technology, Inc.

Technical Specification

510(k) Submission ID K102167
Product Code NTN
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.1500
Decision Date 2010-08-17
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

LO-50 LED LIGHT SOURCE received FDA 510(k) clearance under submission number K102167, sponsored by Fiberoptics Technology, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Gastroenterology, Urology review panel. The statutory decision date of record is 2010-08-17.

Classification & Regulation

This clearance is catalogued under FDA product code NTN and 21 CFR 876.1500, within the Gastroenterology, Urology review panel as a Class II device.