meddevicedb.com FDA Device Reference

BARD HYDROGEL-COATED DIAGNOSTIC URETHRAL CATHETERS

K910196 Class II Traditional
Decision Date
1991-03-27
Sponsor / Applicant
C.R. Bard, Inc.

Technical Specification

510(k) Submission ID K910196
Product Code FGH
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5130
Decision Date 1991-03-27
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BARD HYDROGEL-COATED DIAGNOSTIC URETHRAL CATHETERS received FDA 510(k) clearance under submission number K910196, sponsored by C.R. Bard, 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 1991-03-27.

Classification & Regulation

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