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: JGZ FDA class 2

O-Phthalaldehyde, Urea Nitrogen

Clinical Chemistry

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O-Phthalaldehyde for Urea Nitrogen is a clinical chemistry test system that uses o-phthalaldehyde reagent to measure blood urea nitrogen (BUN) levels, a key indicator of kidney function and protein metabolism. It is classified as FDA Class 2 (moderate risk), requiring 510(k) premarket notification and adherence to general and special controls. The product code is JGZ, regulated under 21 CFR 862.1770, within the Clinical Chemistry medical specialty. This device is eligible for third-party 510(k) review.

510(k) Clearances

11 matches
K Number
Device Name
ROCHE COBAS READY RENAL PROFILE REAGENT STRIP
COBAS READY BUN REAGENT
CLINISTAT BUN (BLOOD UREA NITROGEN) REAGENT TEST
IQ UREA NITROGEN
PHARMACIA B2-MICRO RIA
BLOOD UREA NITROGEN REAGENT SYS
K.D. COLORIMETRIC BLOOD UREA N2 TEST
UREA NITROGEN, KINETIC
SERALYZER BLOOD UREA NITROGEN(BUN)
BLOOD UREA NITROGEN REAGENT
REAGENT SYSTEM

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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