meddevicedb.com FDA Device Reference

Flexible Video-Uretero-Renoscope SSU System

K212458 Class II Traditional
Decision Date
2022-01-20
Sponsor / Applicant
Karl Storz Endoscopy America

Technical Specification

510(k) Submission ID K212458
Product Code FGB
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.1500
Decision Date 2022-01-20
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Flexible Video-Uretero-Renoscope SSU System received FDA 510(k) clearance under submission number K212458, sponsored by Karl Storz Endoscopy America. 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 2022-01-20.

Classification & Regulation

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