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: CFH FDA class 2

Tetrazolium Int Dye-Diaphorase, Lactate Dehydrogenase

Clinical Chemistry

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The Tetrazolium INT Dye-Diaphorase Lactate Dehydrogenase Test is a clinical chemistry device that measures LDH enzyme activity using a coupled reaction system in which diaphorase reduces a tetrazolium dye (INT) to a colored formazan product in proportion to LDH activity, used in the diagnosis of tissue injury from cardiac, hepatic, or hemolytic conditions. It is classified as FDA Class 2 (moderate risk), though it is exempt from 510(k) premarket notification. The product code is CFH, regulated under 21 CFR 862.1440, within the Clinical Chemistry medical specialty. No special flags apply to this device.

510(k) Clearances

13 matches
K Number
Device Name
SPOTCHEM II LDH TEST
CARESIDE LDH
CLINISTAT LDH REAGENT TEST
IQ LDH
LACTATE DEHYDROGENASE (LDH-L)
LACTATE DEHYDROGENASE (LDH) REAGENT SET
EDC/TITAN GELISO-DOT TOTAL LDH ISOENZYME PROCEDURE
WAKO LDH CII TEST
COLORIMETRIC LDH REAGENT SET
LDH REAGENT SET
HYCEL LDH-INT TEST
LDH-INT TEST
COLORIMETRIC DETERMINATION (LDH)

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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