meddevicedb.com FDA Device Reference

Visera Elite II Video System Center

K202646 Class II Special
Decision Date
2020-10-29
Sponsor / Applicant
Olympus Medical Systems Corp.

Technical Specification

510(k) Submission ID K202646
Product Code FET
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.1500
Decision Date 2020-10-29
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Visera Elite II Video System Center received FDA 510(k) clearance under submission number K202646, sponsored by Olympus Medical Systems Corp.. 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 2020-10-29.

Classification & Regulation

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