meddevicedb.com FDA Device Reference

ABSORBENT, DISPOSABLE URINARY DRAINAGE BAG

K901320 Class II Traditional
Decision Date
1991-01-25
Sponsor / Applicant
Ep Medical, Inc.

Technical Specification

510(k) Submission ID K901320
Product Code KNX
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5250
Decision Date 1991-01-25
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ABSORBENT, DISPOSABLE URINARY DRAINAGE BAG received FDA 510(k) clearance under submission number K901320, sponsored by Ep Medical, 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 1991-01-25.

Classification & Regulation

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