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: JIA FDA class 1

Enzymatic Methods, Galactose

Clinical Chemistry

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Enzymatic Methods for Galactose is a clinical chemistry test system using enzymatic reactions to measure galactose concentration in blood or urine, used in the screening and monitoring of galactosemia and related inborn errors of carbohydrate metabolism. It is classified as FDA Class 1 (lowest risk), subject only to general controls. The product code is JIA, regulated under 21 CFR 862.1310, within the Clinical Chemistry medical specialty. This device is eligible for third-party review where applicable.

510(k) Clearances

9 matches
K Number
Device Name
GSP Neonatal Total Galactose kit
GSP NEONATAL TOTAL GALACTOSE KIT
SPOTCHECK NEONATAL TOTAL GALACTOSE MICROPLATE REAGENT KIT
NEONATAL TOTAL GALACTOSE KIT; NEONTAL TOTAL GALACTOSE KIT, MODELS 3029-0010 AND 3029-110B
QUANTASE TOTAL GALACTOSE SCREENING ASSAY 500 TEST KIT
QUANTASE TOTAL GALACTOSE SCREENING ASSAY
ACCUWELL TOTAL GALACTOSE, MODEL 6010-EGAL
NEONATAL CHEMISTRY SYSTEM, GALACTOSE TEST KIT
IMMUCHEM GAL-MW EA

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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