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: JGY FDA class 1

Colorimetric Method, Triglycerides

Clinical Chemistry

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Colorimetric Method for Triglycerides is a clinical chemistry test system that quantifies serum triglycerides through colorimetric enzymatic reactions, widely used in lipid panels to assess cardiovascular risk, hyperlipidemia, and metabolic syndrome. It is classified as FDA Class 1 (lowest risk), subject only to general controls including proper labeling and manufacturing standards. The product code is JGY, regulated under 21 CFR 862.1705, within the Clinical Chemistry medical specialty. No special flags apply to this device.

510(k) Clearances

22 matches
K Number
Device Name
PICCOLO TRGLYCERIDES-CAPILLARY TEST SYSTEM
PICCOLO TRIGLYCERIDES TEST SYSTEM
BIOSCANNER TRIGLYCERIDES TEST STRIPS
BIOSCANNER TRIGLYCERIDES TEST STRIPS
TRIGLYCERIDES
TRIGLYCERIDES REAGENT
DNA TRIGLYCERIDE PROCEDURE
IL TEST(TM) TRIGLYCERIDE
CHOLESTECH LIPID MONITOR SYST, TRIGLYCERIDES TEST
TRIGLYCERIDE (GPO) REAGENT, UNIVERSAL
DMA TRIGLYCERIDE (GPO) PROCEDURE
TRIGLYCERIDE (GPO) TRINDER REAGENT
CLINISTAT TRIGLYCERIDES REAGENT TEST
TRIGLYCERIDES REAGENT (INT, COLORIMETRIC)
TRIGLYCERIDE REAGENT-TRINDER-GPO
TRIGLYZYME V EIKEN
TRIGLYCERIDE REAGENT (COLOR)
TRIGLYCERIDES TEST (500NM)
ELVI TRIGLYCERIDE
WORTHINGTON TRIGLYCERIDES REAGENT SET
TRIGLYCERIDE C-37 RAPID STAT KIT
TRI-CON TRIGLYCERIDGE REAGENTS

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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