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EVIS EXERA GASTROINTESTINAL VIDEOSCOPE GIF-Q160Z

K011151 Class II Special
Decision Date
2001-05-15
Sponsor / Applicant
The Olympus Optical Co.

Technical Specification

510(k) Submission ID K011151
Product Code FDS
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.1500
Decision Date 2001-05-15
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

EVIS EXERA GASTROINTESTINAL VIDEOSCOPE GIF-Q160Z received FDA 510(k) clearance under submission number K011151, sponsored by The Olympus Optical Co.. The device was reviewed via the Special premarket notification pathway and assigned to the Gastroenterology, Urology review panel. The statutory decision date of record is 2001-05-15.

Classification & Regulation

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