meddevicedb.com FDA Device Reference

4 SURE URINARY DRAIN BAG

K896727 Class II Traditional
Decision Date
1990-02-20
Sponsor / Applicant
The Boston & Pacific Co., Inc.

Technical Specification

510(k) Submission ID K896727
Product Code KNX
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5250
Decision Date 1990-02-20
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

4 SURE URINARY DRAIN BAG received FDA 510(k) clearance under submission number K896727, sponsored by The Boston & Pacific Co., 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 1990-02-20.

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.