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: CDO FDA class 1

Acid, Uric, Uricase (U.V.)

Clinical Chemistry

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The Uricase (UV) Uric Acid Test is a clinical chemistry device that quantifies uric acid in blood or urine by enzymatic oxidation using uricase, with the reaction measured spectrophotometrically in the ultraviolet range, providing a highly specific method for diagnosing and monitoring gout and hyperuricemia. It is classified as FDA Class 1 (lowest risk), subject only to general controls, and is exempt from premarket notification. The product code is CDO, regulated under 21 CFR 862.1775, within the Clinical Chemistry medical specialty. No special flags apply to this device.

510(k) Clearances

31 matches
K Number
Device Name
RANDOX URIC ACID
SIGMA DIAGNOSTICS INFINITY URIC ACID REAGENT, MODELS 684-25, 684-100P, 684-500P, 684-2000P, 683-20, 683-100P
SIGMA DIAGNOSTICS INFINITY URIC ACID REAGENT KIT
URIC ACID
URIC ACID
URIC ACID - INCORPORATING DYNAMIC STABILIZATION TECHNOLOGY - (DST)
OLYMPUS URIC ACID REAGENT
URIC ACID TEST ITEM NUMBER 65422
SYSTEMATE URICACID TEST, TECHNICON RA 1000
SYSTEMATE URIC ACID (URCA) ITEM NUMBER 65422
BIOTROL URIC ACID ENZYMATIQUE UV H.P.
GEMENI URIC ACID U.V.
EMDS URIC ACID (URC A) TESTPACK, ITEM #67664/95
ROCHE REAGENTS REAGENT FOR URIC ACID
URIC ACID 75CDO
ULTRACHEM URIC ACID AIDH
ULTRACHEM URIC ACID AIDH #65047
ULTRACHEM URIC ACID AIDH, #65047
URICASE (U.V.) URIC ACID
UV URIC ACID DETERMINATION
ULTRACHEM URIC ACID ALDH, ITEM #65047
URIC ACID/ALDH
COBAS REAGENTS FOR URIC ACID
CENTRIFICHEM URIC ACID
UV URIC ACID DETERMINATION
ACID REAGENT, URIC SINGLE VIAL
PRINCETON BIOMEDIX URICASE (UV)
MULTISTAT III URIC ACID TEST
STATZYME URIC ACID REAGENT
IN VITRO DIAG. FOR URIC ACID
URIC ACID REAGENT SET

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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