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: CDQ FDA class 2

Urease And Glutamic Dehydrogenase, Urea Nitrogen

Clinical Chemistry

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The Urease and Glutamic Dehydrogenase Urea Nitrogen Test is a clinical chemistry device that measures urea nitrogen by sequential enzymatic reactions involving urease (which converts urea to ammonia) and glutamic dehydrogenase (which consumes NADH proportionally to ammonia released), allowing photometric quantification, used in assessment of renal function. It is classified as FDA Class 2 (moderate risk), requiring 510(k) premarket notification. The product code is CDQ, regulated under 21 CFR 862.1770, within the Clinical Chemistry medical specialty. This device is eligible for third-party review.

510(k) Clearances

50+ matches
K Number
Device Name
Urea Nitrogen2
BS-480 CHEMISTRY ANALYZER, BS-490 CHEMISTRY ANALYZER, CLC720I CHEMISTRY ANALYZER
EASYRA UREA NITROGEN AND CREATININE REAGENTS
UREA/BUN, SCAL, NORTROL, ABTROL
ABX PENTRA GLUCOSE HK CP, UREA CP, URIC ACID CP
TECO CX3 REAGENT SET FOR SYNCHRON CX SYSTEM
RAICHEM BUN RATE REAGENT (LIQUID)
PRECISION SYSTEMS ANALETTE CHEMISTRY ANALYZER STANBIO LABORATORY REAGENTS
ATAC PAK BUN REAGENT
RAICHEM BUN RATE REAGENT
WIENER LAB. UREA UV CINETICA AA
UREA NITROGEN (BUN) LIQUID REAGENT
UREA-L3K ASSAY, CATALOGUE NUMBER 283-17/30
ATAC PAK BUN REAGENT AND ATAC CALIBRATOR KITS
WAKO L-TYPE UN TEST
UREA-L3K ASSAY, CATALOGUE NUMBER 283-17/10/30/50
SIGMA DIAGNOSTICS INFINITY BUN REAGENT, MODELS 63-25, 63-100P, 63-500P, 63-2000P, 64-20, 64-100P
BUN, MODEL BU 104-01
SIGMA DIAGNOSTICS INFINITY BUN REAGENT KIT
UREA
UREA
UREA NITROGEN (BUN) LIQUID REAGENT
CARESIDE BUN
IL TEST UREA NITROGEN
UREA-SL ASSAY CATALOGUE NUMBER 239-10, 239-30
UREA
BUN (LIQUID) REAGENT SET
BUN
UREA (UREA NITROGEN) - INCORPORATING DYNAMIC STABILIZATION TECHNOLOGY (DST)
UREA NITROGEN (BUN) LIQUI-UV
HICHEM BUN/UREA REAGENT KIT
ROCHE REAGENT FOR BUN
BLOOD UREA NITROGEN REAGENT SYSTEM
BUN REAGENT
UREA NITROGEN REAGENT
BUN-300/BUN-500 UREA NITROGEN REAGENT
UREA KIT
UREA NITROGEN TEST ITEM NUMBER 65408
OLYMPUS REPLY UREA NITROGEN REAGENT
UREA NITROGEN TEST
OLYMPUS BUN REAGENT
MILES URINE UREA NITROGEN METHOD
OLYMPUS UREA NITROGEN (BUN) REAGENT
IL TEST(TM) UREA NITROGEN
SYNERMED UREA NITROGEN REAGENT KIT
ECLIPSE ICA BUN
UREA NITROGEN TEST
COULTER UREA NITROGEN REAGENT
CHEM 1 CLINICAL ANALYZER URINE UREA NITROGEN
AMRESCO BUN-KINETIC REAGENTS PRODUCTS #7583

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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