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FLEXIBLE AND RIGID URETEROTOME SYSTEM

K904939 Class II Traditional
Decision Date
1992-01-07
Sponsor / Applicant
Olympus Corp.

Technical Specification

510(k) Submission ID K904939
Product Code EZO
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.4770
Decision Date 1992-01-07
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

FLEXIBLE AND RIGID URETEROTOME SYSTEM received FDA 510(k) clearance under submission number K904939, sponsored by Olympus Corp.. 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 1992-01-07.

Classification & Regulation

This clearance is catalogued under FDA product code EZO and 21 CFR 876.4770, within the Gastroenterology, Urology review panel as a Class II device.