meddevicedb.com FDA Device Reference

ENTERIC INJECTION CATHETER WITH IRRIGATION

K002778 Class II Traditional
Decision Date
2000-11-22
Sponsor / Applicant
Enteric Medical Technologies, Inc.

Technical Specification

510(k) Submission ID K002778
Product Code FBK
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.1500
Decision Date 2000-11-22
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ENTERIC INJECTION CATHETER WITH IRRIGATION received FDA 510(k) clearance under submission number K002778, sponsored by Enteric Medical 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 2000-11-22.

Classification & Regulation

This clearance is catalogued under FDA product code FBK and 21 CFR 876.1500, within the Gastroenterology, Urology review panel as a Class II device.