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: JHM FDA class 1

Colorimetric Method, Lipoproteins

Clinical Chemistry

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Colorimetric Method for Lipoproteins is a clinical chemistry test system employing colorimetric reactions to quantify lipoprotein fractions such as HDL and LDL in serum, used in lipid profiling and assessment of cardiovascular risk. It is classified as FDA Class 1 (lowest risk), subject only to general controls including proper labeling and manufacturing standards. The product code is JHM, regulated under 21 CFR 862.1475, within the Clinical Chemistry medical specialty. No special flags apply to this device.

510(k) Clearances

9 matches
K Number
Device Name
PICCOLO HDL-CAPILLARY TEST SYSTEM
DIMENSION VISTA HDLC FLEX REAGENT CARTRIDGE
DIMENSION AHDL FLEX REAGENT CARTRIDGE, MODEL: DF48B
DIMENSION AUTOMATED HDL CHOLESTEROL (AHDL) FLEX REAGENT CARTRIDGE (DF48A) CATALOG # DF48A
LDL CHOLESTEROL (AUTOMATED)
DIMENSION AUTOMATED HIGH DENSITY LIPOPROTEIN CHOLESTEROL (ADHL) FLEX REAGENT CARTRIDGE
ROCHE COBAS READY HDL CHOLESTEROL REAGENT
HDL PRECIPITANT REAGENT SET
LYPOPROTEIN CHOLESTEROL TEST KIT

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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