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: JXE FDA class 2

Device, Nerve Conduction Velocity Measurement

Neurology

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Device, Nerve Conduction Velocity Measurement is a neurological diagnostic device used to assess the speed at which electrical signals travel along peripheral nerves, supporting the evaluation of conditions such as peripheral neuropathy, carpal tunnel syndrome, and Guillain-Barre syndrome. It is classified as FDA Class 2, indicating moderate risk and requiring 510(k) premarket notification. The product code is JXE, regulated under 21 CFR 882.1550, and falls within the Neurology medical specialty. This device is eligible for third-party review.

510(k) Clearances

27 matches
K Number
Device Name
NM-01/CPT neurometer (NM-01/CPT)
Mediracer NCS
NEUROMETRIX ADVANCE
NC-STAT
XLTEK NEUROPATH, MODEL PK1070
VIRTUAL MEDICAL SYSTEMS MODEL VT3000
MODIFICATION TO NC-STAT
MODIFICATION OF NC-STAT
MODIFICATION TO:BREVIO NERVE CONDUCTION TEST INSTRUMENT
NC-STAT
NEURO SCAN MEDICAL STSTEMS, MODEL MEDICOR 8
MODIFICATION TO NC-STAT
NC-STAT
NERVEPACE(R) NERVE CONDUCTION VIEWSCOPE (200VS)
INSTA-NERVE(TM) NERVE CONDUCTION MONITOR
TD50 ELECTROMYOGRAPH
SMARTSCOPE
REUSABLE DUAL DISC BAR RECORDING ELECTRODES
REUSABLE DUAL DISC BAR ELECTRODES, VARIOUS MODELS
SENSORY NERVE CONDUCTION VELOCITY TESTING UNIT
EMG OPTION FOR MICROSHEV 4000
IMPULSE EPIDURAL ELECTRODE
DIGITAL ELECTRONEUROMETER S-100
EMG REPORT GENERATOR
GRASS MODEL NL FACIAL NERVE LOCATOR & MONITOR
CADWELL 5200
NERVEL-NERVE CONDUCTION VELOCITY METER

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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