meddevicedb.com FDA Device Reference

BALLOON URETERAL DILATORS, ACCENT DG BALLOON URETERAL DILATOR SET, ASCEND BALLOON DILATION CATHETERS, BALLOON DILATION C

K990072 Class II Traditional
Decision Date
1999-03-25
Sponsor / Applicant
Cook Urological, Inc.

Technical Specification

510(k) Submission ID K990072
Product Code EZN
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5470
Decision Date 1999-03-25
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BALLOON URETERAL DILATORS, ACCENT DG BALLOON URETERAL DILATOR SET, ASCEND BALLOON DILATION CATHETERS, BALLOON DILATION C received FDA 510(k) clearance under submission number K990072, sponsored by Cook Urological, 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 1999-03-25.

Classification & Regulation

This clearance is catalogued under FDA product code EZN and 21 CFR 876.5470, within the Gastroenterology, Urology review panel as a Class II device.