Cleared Traditional

K884609 - EURO-COLLINS SOLUTION SETS

K884609 is an FDA 510(k) clearance for EURO-COLLINS SOLUTION SETS, manufactured by Fresenius USA, Inc.. The device is a Class 2 Gastroenterology & Urology device with product code KDL cleared through the Traditional 510(k) pathway after a 80-day FDA review.

K884609 · Fresenius USA, Inc. · Gastroenterology & Urology device
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Jan 1989
Decision
80d
Days
Class 2
Risk

K884609 is an FDA 510(k) clearance for the EURO-COLLINS SOLUTION SETS. Classified as Set, Perfusion, Kidney, Disposable (product code KDL), Class II - Special Controls.

Submitted by Fresenius USA, Inc. (Germany, DE). The FDA issued a Cleared decision on January 26, 1989 after a review of 80 days - a notably fast clearance cycle.

This device falls under the Gastroenterology & Urology FDA review panel, regulated under 21 CFR 876.5880 - 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 Fresenius USA, Inc. devices

FDA 510(k) Submission Details - K884609

510(k) Number K884609 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received November 07, 1988
Decision Date January 26, 1989
Days to Decision 80 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
50d faster than avg
Panel avg: 130d · This submission: 80d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

KDL Device Classification - Class 2, Special Controls

Product Code KDL Set, Perfusion, Kidney, Disposable
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 876.5880
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.

Regulatory Peers - KDL Set, Perfusion, Kidney, Disposable

All 8
Devices cleared under the same product code (KDL) and FDA review panel - the closest regulatory comparables to K884609.
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K780470 · Dow Corning Corp. Healthcare Industries Materials · Apr 1978
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K760922 · Shiley, Inc. · Nov 1976