Cleared Traditional

K904992 - MINNILERT AIR DETECTOR

K904992 is an FDA 510(k) clearance for MINNILERT AIR DETECTOR, manufactured by Minntech Corp.. The device is a Class 2 Gastroenterology & Urology device with product code FJF cleared through the Traditional 510(k) pathway after a 90-day FDA review.

K904992 · Minntech Corp. · Gastroenterology & Urology device
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Feb 1991
Decision
90d
Days
Class 2
Risk

K904992 is an FDA 510(k) clearance for the MINNILERT AIR DETECTOR. Classified as Detector, Air Bubble (product code FJF), Class II - Special Controls.

Submitted by Minntech Corp. (Minneapolis, US). The FDA issued a Cleared decision on February 5, 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 876.5820 - 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 Minntech Corp. devices

FDA 510(k) Submission Details - K904992

510(k) Number K904992 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received November 07, 1990
Decision Date February 05, 1991
Days to Decision 90 days
Submission Type Traditional
Review Panel Gastroenterology & Urology (GU)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
41d faster than avg
Panel avg: 131d · This submission: 90d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

FJF Device Classification - Class 2, Special Controls

Product Code FJF Detector, Air Bubble
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 876.5820
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most Gastroenterology & Urology devices follow this clearance model.