meddevicedb.com FDA Device Reference

OES ELITE Telescopes, Protective Tube

K151191 Class II Traditional
Decision Date
2015-11-24
Sponsor / Applicant
Olympus Winter & Ibe GmbH

Technical Specification

510(k) Submission ID K151191
Product Code FBP
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.1500
Decision Date 2015-11-24
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

OES ELITE Telescopes, Protective Tube received FDA 510(k) clearance under submission number K151191, sponsored by Olympus Winter & Ibe GmbH. 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 2015-11-24.

Classification & Regulation

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