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: GWS FDA class 1

Analyzer, Spectrum, Electroencephalogram Signal

Neurology

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The Analyzer, Spectrum, Electroencephalogram Signal is a neurological device that performs spectral frequency analysis of EEG signals, transforming raw brainwave data into frequency components to assist in the evaluation of neurological conditions such as epilepsy, encephalopathy, and sleep disorders. It is an FDA Class 1 device subject to general controls only, with no premarket submission required. This device is eligible for third-party 510(k) review. Regulated under 21 CFR 882.1420 with product code GWS in the Neurology specialty.

510(k) Clearances

15 matches
K Number
Device Name
PERSYST PRISM
EEG ANALYZER
RHYTHM
NICOLET BEAM II SYSTEM
ISTAT SOFTWARE
STD-228 SPECTRAL TREND DISPLAY
OEE_7102 EEG/TREND MONITOR
CNS 4/8 AND CT 48.1 SOFTWARE
CNS-16 & LTM 1.0 SOFTWARE
NEUROSCIENCE MAP-10 EEG
NEUROLAB II
CEREBRAL TRACER 1500 & CT 1.0 SOFTWARE
MEUROMETRICS MONITOR
NEUROMETRICS MONITOR
MINI-CEARS COMPUTER (MODEL 1)

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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