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: JPZ FDA class 1

Colorimetric Method, Gamma-Glutamyl Transpeptidase

Clinical Chemistry

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The Colorimetric Method, Gamma-Glutamyl Transpeptidase test is a clinical chemistry diagnostic reagent used to measure gamma-glutamyl transpeptidase (GGT) activity in serum by a colorimetric reaction, providing an enzymatic marker used in the evaluation of hepatic and biliary disease, as well as monitoring of alcohol use. This device is FDA Class 1, the lowest risk category, requiring only general controls and no premarket submission. It carries product code JPZ and is regulated under 21 CFR 862.1360, within the Clinical Chemistry medical specialty.

510(k) Clearances

33 matches
K Number
Device Name
CARESIDE GGT
DMA GAMMA GLUTAMYLTRANSFERASE (GGT) PROCEDURE
GAMMA-GT
KING DIAGNOSTICS GAMMA GT REAGENT
GGT REAGENT
ROCHE COBAS READY GGT REAGENT
ELITECH GAMMA GT TEST KIT
WAKO(TM) AUTOKIT GAMMA-GT
GAMMA GLUTAMYL TRANSFERASE REAGENT SET
MULTICHEM(R) Y -GLUTAMYLTRANSFERASE (Y -GT)
GAMMA GLUTAMYLTRANSFERASE REAGENT
VISION (TM) GGTP
GAMMA GLUTAMYL TRANSFERASE PROCEDURE
GAMMA GLUTAMYL TRANSFERASE PROCEDURE
G.T. (GAMMA-GLUTAMYL TRANSFERASE) REAGENT
GAMMA GLUTAMYL TRANSPEPTIDASE (GGTP) REAGENT SET
GAMMA GLUTAMYL TRANSPEPTIDASE (KINECTIC)REAGENTSET
GAMMA GLUTAMYL TRANSPEPTIDASE REAGENT SET
GLUTAMYLTRANSFERASE ASSAY KIT
TOYO JOZO G-GTP TEST
WAKO R-GTP C-TEST
RAICHEM & GT REAGENT
GILCHEM Y-GT REAGENT
ULTRAZYME PLUS 2GT
ULTRAZYME PLUS-GT, #64959 & 65032
GAMMA-GLUTAMYL TRANSPEPTIDASE (GGT)
COULTER ACCU-ZYME IIY-GT REAGENT KIT
SMA/GGT
ULTRAZYME PLUS GT
REAGENT SYSTEM (NO. SC 135)
REAGENT, Y-GT MAX-PACK
ASSAY FOR GAMMA GLUTAMYLTRANSFERASE
ULTRAZYME GT

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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