meddevicedb.com FDA Device Reference

BAG, LEG, URINE COLLECTING DEVICE

K760069 Class II Traditional
Decision Date
1976-10-20
Sponsor / Applicant
Pharmaseal Div., Baxter Healthcare Corp.

Technical Specification

510(k) Submission ID K760069
Product Code KNX
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5250
Decision Date 1976-10-20
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BAG, LEG, URINE COLLECTING DEVICE received FDA 510(k) clearance under submission number K760069, sponsored by Pharmaseal Div., Baxter Healthcare Corp.. 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 1976-10-20.

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.