meddevicedb.com FDA Device Reference

TRIP(TM) NASOGASTRIC SUMP CATHETER

K911825 Class I Traditional
Decision Date
1991-07-23
Sponsor / Applicant
Tonometrics, Inc.

Technical Specification

510(k) Submission ID K911825
Product Code FFT
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.1400
Decision Date 1991-07-23
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TRIP(TM) NASOGASTRIC SUMP CATHETER received FDA 510(k) clearance under submission number K911825, sponsored by Tonometrics, 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 1991-07-23.

Classification & Regulation

This clearance is catalogued under FDA product code FFT and 21 CFR 876.1400, within the Gastroenterology, Urology review panel as a Class I device.