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: OMC FDA class 2

Reduced- Montage Standard Electroencephalograph

Neurology

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The Reduced-Montage Standard Electroencephalograph (product code OMC) is a Class 2 neurological device regulated under 21 CFR 882.1400 in the Neurology specialty (NE), cleared via 510(k). It acquires, displays, stores, and archives electroencephalographic signals from the brain using a user-specified or sponsor-specified reduced electrode array of fewer than 16 electrodes, as distinct from full-montage EEG systems. The device is eligible for third-party review and is not an implant or life-sustaining device.

510(k) Clearances

26 matches
K Number
Device Name
REMI Remote EEG Monitoring System
Natus BrainWatch System
QUEX ED; QUEX S
SignalNED System (Model RE)
REMI Remote EEG Monitoring System
NEBA® Compact EEG2R Mobile Headset
Neurosteer EEG Recorder
REMI
Byteflies Kit
AE-120A EEG Head Set
Ceribell Pocket EEG Device
X8 System - Sleep Profiler (SP40), X8 System - Sleep Profiler PSG2 (SP29), X8 System - Stat X8 (XS29)
IEEG
X4 SYSTEM
X4
ENTERPRISE ELECTROPHYSIOLOGY SYSTEM
NeuroWave NeuroFAST MONITORING SYSTEM, MODEL NF-701
NEUROPORT NEURAL SIGNAL PROCESSING SYSTEM
BIOSOMNIA-V3
ENVOY PATIENT MONITOR
BIOSOMNIA
OLYMPIC MEDICAL LECTROMED CEREBRAL FUNCTION MONITOR SYSTEM, MODEL 5330
CRYSTAL MONITOR MODEL 16
CRYSTAL-EEG MODEL 15
CRYSTAL-EEG MODEL 10 (MODEL 10)
ACCESSORY TO ECG ANALYSIS SYS.

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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