Cleared Traditional

K911825 - TRIP(TM) NASOGASTRIC SUMP CATHETER

K911825 is an FDA 510(k) clearance for TRIP(TM) NASOGASTRIC SUMP CATHETER, manufactured by Tonometrics, Inc.. The device is a Class 1 Gastroenterology & Urology device with product code FFT cleared through the Traditional 510(k) pathway after a 90-day FDA review.

K911825 · Tonometrics, Inc. · Gastroenterology & Urology device
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Jul 1991
Decision
90d
Days
Class 1
Risk

K911825 is an FDA 510(k) clearance for the TRIP(TM) NASOGASTRIC SUMP CATHETER. Classified as Electrode, Ph, Stomach (product code FFT), Class I - General Controls.

Submitted by Tonometrics, Inc. (Bethesda, US). The FDA issued a Cleared decision on July 23, 1991 after a review of 90 days - within the typical 510(k) review window.

This device falls under the Gastroenterology & Urology FDA review panel, regulated under 21 CFR 876.1400 - the FDA gastroenterology and urology device framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Gastroenterology & Urology review framework, consistent with the majority of Class II 510(k) submissions.

View all Tonometrics, Inc. devices

FDA 510(k) Submission Details - K911825

510(k) Number K911825 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 24, 1991
Decision Date July 23, 1991
Days to Decision 90 days
Submission Type Traditional
Review Panel Gastroenterology & Urology (GU)
Summary Statement
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
40d faster than avg
Panel avg: 130d · This submission: 90d
Pathway characteristics
Predicate-based equivalence.

FFT Device Classification - Class 1, General Controls

Product Code FFT Electrode, Ph, Stomach
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 876.1400
What this classification means

Class I devices are subject to general controls only and most are exempt from 510(k) premarket notification. They represent the lowest regulatory burden in the FDA device framework.

Regulatory Peers - FFT Electrode, Ph, Stomach

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