Cleared Traditional

CLEANING BRUSH (K874239) - FDA 510(k) Clearance

Class I Gastroenterology & Urology device.

K874239 · Endovations · Gastroenterology & Urology device
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Dec 1987
Decision
74d
Days
Class 1
Risk

K874239 is an FDA 510(k) clearance for the CLEANING BRUSH. Classified as Accessories, Cleaning Brushes, For Endoscope (product code MNL), Class I - General Controls.

Submitted by Endovations (Camp Hill, US). The FDA issued a Cleared decision on December 29, 1987 after a review of 74 days - a notably fast clearance cycle.

This device falls under the Gastroenterology & Urology FDA review panel, regulated under 21 CFR 876.1500 - 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: Fast-track predicate clearance. Standard predicate reliance. The short review cycle indicates strong predicate alignment - the FDA found sufficient equivalence without extended technical review.

View all Endovations devices

Submission Details

510(k) Number K874239 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received October 16, 1987
Decision Date December 29, 1987
Days to Decision 74 days
Submission Type Traditional
Review Panel Gastroenterology & Urology (GU)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
56d faster than avg
Panel avg: 130d · This submission: 74d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code MNL Accessories, Cleaning Brushes, For Endoscope
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 876.1500
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.