meddevicedb.com FDA Device Reference

AQ HYDROPHILIC UROLOGICAL CATHETERS

K962004 Class II Traditional
Decision Date
1996-06-11
Sponsor / Applicant
Cook Urological, Inc.

Technical Specification

510(k) Submission ID K962004
Product Code EYB
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5130
Decision Date 1996-06-11
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

AQ HYDROPHILIC UROLOGICAL CATHETERS received FDA 510(k) clearance under submission number K962004, 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 1996-06-11.

Classification & Regulation

This clearance is catalogued under FDA product code EYB and 21 CFR 876.5130, within the Gastroenterology, Urology review panel as a Class II device.