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: KNK FDA class 1

Acid, Uric, Uricase (Colorimetric)

Clinical Chemistry

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The Uric Acid Uricase Colorimetric test is an in vitro diagnostic assay used in clinical chemistry laboratories to measure uric acid concentrations in blood or urine using the uricase enzymatic colorimetric method, supporting the diagnosis and monitoring of gout, hyperuricemia, and related metabolic conditions. It is classified as FDA Class 1, indicating low risk subject to general controls with no premarket submission required. The product code is KNK and the applicable regulation is 21 CFR 862.1775 in the Clinical Chemistry specialty.

510(k) Clearances

50+ matches
K Number
Device Name
URIC ACID MODEL 3P39
OLYMPUS URIC ACID REAGENT, MODEL OSR6X98
VITALAB URIC ACID REAGENT
ATAC PAK URIC ACID REAGENT AND ATAC CALIBRATOR
URIC ACID ASSAY FOR THE ADVIA INTEGRATED MODULAR SYSTEM
WIENER LAB URICOSTAT ENZIMATICO AA LIQUIDA
JAS URIC ACID LIQUID REAGENT
WIENER LAB. URICOSTAT ENZIMATICO AA, MODELS 2X50 ML CATALOGUE NO 1840106 AND 4X50 ML CATALOGUE NO 1840105
WAKO L-TYPE UA F TEST
URIC ACID, MODEL UA112-01
CARESIDE URIC ACID
SYNCHRON CX SYSTEMS URIC ACID (URIC) REAGENT
URIC ACID REAGENT
URIC, UA, OR URIC ACID
URIC ACID (LIQUID) REAGENT SET
URIC ACID-SL ASSAY CATALOGUE NO. 237-60
URIC ACID CATALOGE# 220-93/94/97
URIC ACID QVET
KODAK EKTACHEM CLINICAL CHEMISTRY SLIDES (URIC)
IL TEST URIC ACID
URIC ACID ENZYMATIC COLORIMERIC KIT
OLYMPUS URIC ACID REAGENT
SYNERMED 600 NM URIC ACID REAGENT KIT
MILES AUTO METH DETERMIN OF URIC ACID IN URINE
OLYMPUS URIC ACID REAGENT
ROCHE REAGENT FOR URIC ACID--MODIFICATION
URIC ACID REAGENT SET
URIC ACID (URICASE) REAGENT, UNIVERSAL
ABBOTT QUICKSTART URIC ACID TEST (URCA) ITEM# 5A34
SYNERMED URIC ACID REAGENT KIT
COBAS READY PROFILE 2 REAGENT STRIP
URIC ACID TEST KIT
WAKO(TM) AUTOKIT URIC ACID
TECHNICON CHEM 1 CLINICAL ANALYZER FOR URINE URIC
COULTER URIC ACID REAGENT
ABBOTT SPECTRUM URIC ACID REAGENT KIT
MODIFIED PARAMAX URIC ACID REAGENT
COBAS READY URIC ACID REAGENT
URIC ACID FOR MANUAL/AUTOMATED APPLICATIONS
URIC ACID PAP
ROCHE REAGENT FOR URIC ACID
URIC ACID TEST ITEM NUMBER 65422
URIC ACID REAGENT (PROCEDURE NUMBER 686)
AMRESCO URIC ACID REAGENTS #7628
URIC ACID KIT, CODES 4825400 AND 4825050
URIC ACID TEST (URIC) ITEM #65620
BIOTROL URIC ACID ENZYMATIQUE TRINDER
URIC ACID REAGENT (PRODUCT #88219)
URIC ACID REAGENT SET
WAKO AUTOKIT URIC ACID

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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