meddevicedb.com FDA Device Reference

NORTHGATE FLOW ASSIST TUBING FOR UROLOGY

K943361 Class II Traditional
Decision Date
1995-09-29
Sponsor / Applicant
Northgate Technologies, Inc.

Technical Specification

510(k) Submission ID K943361
Product Code LJH
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5130
Decision Date 1995-09-29
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

NORTHGATE FLOW ASSIST TUBING FOR UROLOGY received FDA 510(k) clearance under submission number K943361, sponsored by Northgate Technologies, 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 1995-09-29.

Classification & Regulation

This clearance is catalogued under FDA product code LJH and 21 CFR 876.5130, within the Gastroenterology, Urology review panel as a Class II device.