meddevicedb.com FDA Device Reference

E-Brik Visualization Assistant

K221293 Class II Traditional
Decision Date
2022-07-07
Sponsor / Applicant
Jdi Surgical, Inc.

Technical Specification

510(k) Submission ID K221293
Product Code OCT
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.1500
Decision Date 2022-07-07
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

E-Brik Visualization Assistant received FDA 510(k) clearance under submission number K221293, sponsored by Jdi Surgical, 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 2022-07-07.

Classification & Regulation

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