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: KZQ FDA class 1

Chromatography(Gas), Clinical Use

Clinical Chemistry

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The Clinical Use Gas Chromatography system is a laboratory analytical instrument used in clinical chemistry to separate and identify compounds in biological samples, such as measuring drug concentrations, detecting volatile compounds, or profiling metabolites, based on their differential migration through a stationary phase under a carrier gas. It is classified as FDA Class 1, the lowest risk category, subject to general controls only, with no premarket submission required. The product code is KZQ, regulated under 21 CFR 862.2250, in the Clinical Chemistry medical specialty. No special flags apply to this device.

510(k) Clearances

12 matches
K Number
Device Name
8000 SERIES GAS CHROMATOGRAPHS
VARIAN 3300 & 3400 GAS CHROMATOGRAPHS
GAS CHROMATOGRAPH 5890A
HS-100 HEADSPACE SAMPLING ACCESSORY
SIGMA 300 GAS CHROMATROGRAPH
SIGMA 2000 GAS CHROMATOGRAPH
TRACE ANALYTICAL REDUCTION GAS ANALYZ
MODEL 5790 GAS CHROMATOGRAPH
VISTA 44 GAS CHROMATOGRAPHY ANALYSIS
5880 SERIES OF GAS CHROMATOGRAPHS
DETECTOR, IR, MODEL GC-33
GAS CHROMOTOGRAPHS, SIGMA 1,2,3,4,&10

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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