Tool · 510(k)

510(k) Predicate Finder

Find potential predicate devices for your 510(k) submission. Enter a K-number to find all clearances with the same product code, a three-letter product code to browse clearances directly, or search by device name.

Product Code: KQO FDA class 1

Automated Urinalysis System

Clinical Chemistry

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This device is an automated urinalysis system used to analyze urine samples for physical, chemical, and microscopic characteristics, supporting the diagnosis of urinary tract infections, kidney disease, diabetes, and other conditions. It is classified as FDA Class 1, the lowest risk category, subject to general controls only. The product code is KQO, regulated under 21 CFR 862.2900 within the Clinical Chemistry specialty. No special flags apply.

510(k) Clearances

46 matches
K Number
Device Name
URISCAN OPTIMA
Mission U120 Ultra Urine Analyzer, Mission Liquid Urine Controls, Mission Liquid Diptube Urine Control
CLINITEK NOVUS; AUTOMATED URINE CHEMISTRY ANALYZER, 10 URINALYSIS CASSETTE, CALIBRATION KIT
AUTION HYBRID AU-4050 FULLY AUTOMATED INTEGRATED URINE ANALYZER SYSTEM; URIFLET S 9HA URINE TEST STRIPS; AUTION CONTROL
CYBOW READER, MODELS 300 & 720
CHEM VELOCITY AUTOMATED URINE CHEMISTRY SYSTEM, STRIPS AND CALCHEK KIT
URITEST 50 AND URITEST 500 URINE ANALYZER
COBAS U411 TEST SYSTEM
AUTION MAX MODEL AX-4030 URINALYSIS SYSTEM
ACON U120 URINE ANALYZER, MODEL U111-101
HEMOCUE ALBUMIN 201 ANALYZING SYSTEM
URITEK-720+ URINE ANALYZER
URITEK 151 URINE ANALYZER, MODEL TC-151
BAYER CLINITEK STATUS ANALYZER
AUTION JET AJ-4270 URINE ANALYZER
AUTION MAX AX-4280 URINALYSIS SYSTEM
STRIPMAX 1210 URINE CHEMISTRY ANALYZER, URIMATE REAGENT STRIP FOR URINALYSIS
CHEMSTRIP 101 URINE ANALYZER
URISCAN S-300 SEMI-AUTOMATED URINE CHEMISTRY ANALYZER
THE YELLOW IRIS URINALYSIS WORKSTATION
STC DIAGNOSTICS AUTO-LYTE URINARY LEUKOCYTE ESTERASE ASSAY
UA PERFECT AUTOMATED ANALYSIS ASSAY FOR UROBILLINOGEN IN URINE
CLINITEK 50 URINE CHEMISTRY ANALYZER
AUTOMATED ANALYSIS ASSAY FOR BILIRUBIN IN URINE
STC DIAGNOSTICS AUTO-LYTE PH ASSAY
900UDX URINE PATHOLOGY SYSTEM
CHEMSTRIP CRITERION URINE ANALYZER
CLINITEK ATLAS AUTOMATED URINE CHEMISTRY ANALYZER
CHEMSTRIP MINI UA URINE ANALYZER
THE YELLOW IRIS
UA PERFECT
CHEMSTRIP SUPER UA URINE ANALYZER
CLINITEK ATLAS AUTOMATED URINE CHEMISTRY SYSTEM
CHEMSTRIP URINE ANALYZER
CLINITEK 200+ URINE CHEMISTRY ANALYZER
CHEMSTRIP URINE ANALYZER
SUPER URINE ANALYZER SYSTEM
CLINI-TEK AUTO 2000 REFLECTANCE SPECTR
CLINITEK 200 SEMI-AUTOMATED URINALYSIS
CLINITEK 10 SEMI-AUTO URINALYSIS SYS
URINE ANALYZER SYSTEM
YELLOW IRIS TM
CLINI-TEK SEMI-AUTOMATED URINALYSIS SYST
AUTOMATED URINALYSIS SYSTEM
CLINILAB AUTOMATED URINALYSIS SYSTEM
INSTRUMENTED SYSTEM FOR URINALYSIS

What is a Predicate Device?

A predicate device is a legally marketed device that a new 510(k) applicant uses to demonstrate substantial equivalence. The FDA's 510(k) pathway requires manufacturers to show that their device has the same intended use and similar technological characteristics as one or more predicate devices already cleared for commercial distribution.

Finding the right predicate is a critical step in 510(k) strategy. Manufacturers typically search for cleared devices with the same FDA product code, which groups devices by their intended use and regulatory classification. This tool helps you identify potential predicates by browsing all clearances within a product code.

Note that predicate devices must be legally marketed — they cannot be devices that were cleared but never commercialized, or devices subject to a mandatory recall. The determination of substantial equivalence considers intended use, technological characteristics, and performance data.

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