meddevicedb.com FDA Device Reference

EVIS EUS Ultrasound Gastrointestinal Videoscope (Olympus GF-UE190)

K261183 Class II Traditional
Decision Date
2026-07-31
Sponsor / Applicant
Olympus Medical Systems Corporation

Technical Specification

510(k) Submission ID K261183
Product Code ODG
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.1500
Decision Date 2026-07-31
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

EVIS EUS Ultrasound Gastrointestinal Videoscope (Olympus GF-UE190) received FDA 510(k) clearance under submission number K261183, sponsored by Olympus Medical Systems Corporation. 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 2026-07-31.

Classification & Regulation

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