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: KLX FDA class 2

Electroglottograph

Ear, Nose, Throat

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An Electroglottograph is a non-invasive diagnostic instrument used in ear, nose, and throat medicine to assess vocal fold contact and vibration patterns by measuring electrical impedance changes at the larynx level, aiding in the evaluation of voice disorders. It is classified as FDA Class 2, indicating moderate risk requiring 510(k) premarket clearance. The product code is KLX and it is regulated under 21 CFR 874.1325 in the Ear, Nose, and Throat specialty.

510(k) Clearances

4 matches
K Number
Device Name
ELECTROGLOTTOGRAPH
ELECTROGLOTTOGRAPH
GLOTTAL FREQUENCY ANALYSER
ELECTROGLOTTOGRAPH NAKED EGG BOXED EGG

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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