meddevicedb.com FDA Device Reference

BAG, URINARY, DRAINAGE, 2D9013

K770762 Class II Traditional
Decision Date
1977-05-10
Sponsor / Applicant
Travenol Laboratories, S.A.

Technical Specification

510(k) Submission ID K770762
Product Code KNX
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5250
Decision Date 1977-05-10
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BAG, URINARY, DRAINAGE, 2D9013 received FDA 510(k) clearance under submission number K770762, sponsored by Travenol Laboratories, S.A.. 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 1977-05-10.

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.