meddevicedb.com FDA Device Reference

DISPOSABLE UROSTOMY POUCH

K850750 Class I Traditional
Decision Date
1985-05-23
Sponsor / Applicant
Biolog, Inc.

Technical Specification

510(k) Submission ID K850750
Product Code EXB
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5900
Decision Date 1985-05-23
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DISPOSABLE UROSTOMY POUCH received FDA 510(k) clearance under submission number K850750, sponsored by Biolog, 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 1985-05-23.

Classification & Regulation

This clearance is catalogued under FDA product code EXB and 21 CFR 876.5900, within the Gastroenterology, Urology review panel as a Class I device.