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SELF RETAINING MALE EXTERNAL URINARY CATHETER

K962900 Class I Traditional
Decision Date
1996-09-16
Sponsor / Applicant
Hollister, Inc.

Technical Specification

510(k) Submission ID K962900
Product Code EXJ
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5250
Decision Date 1996-09-16
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SELF RETAINING MALE EXTERNAL URINARY CATHETER received FDA 510(k) clearance under submission number K962900, sponsored by Hollister, 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 1996-09-16.

Classification & Regulation

This clearance is catalogued under FDA product code EXJ and 21 CFR 876.5250, within the Gastroenterology, Urology review panel as a Class I device.