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: GWL FDA class 2

Amplifier, Physiological Signal

Neurology

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The Amplifier, Physiological Signal is a neurological device that amplifies weak bioelectrical signals from the body, such as electroencephalographic (EEG) or electromyographic (EMG) signals, to enable their recording and interpretation during neurological testing. It is an FDA Class 2 device, reflecting moderate risk and requiring 510(k) premarket clearance. The product code is GWL, regulated under 21 CFR 882.1835 in the Neurology specialty. This device is eligible for third-party 510(k) review.

510(k) Clearances

50+ matches
K Number
Device Name
Delphi Amplifier
NExT Station; NExT Station Advanced
DreamClear
BE Plus PRO, Neurotravel LIGHT
X-trodes System M
Vlab
SomniCheck
NomadAir PMU810
Quick-20m
Digital NeuroPort Biopotential Signal Processing System
8-CH Electroencephalography Amplifier
eego amplifiers
Sienna Ultimate Wireless Amplifier
g.Nautilus PRO
R-40 EEG Amplifier
NEMUS 2 SYSTEM
g.HIamp
BE PLUS LTM AMPLIFIER GWI AMPLIFIER
NICOLET WIRELESS EEG
NOMAD SLEEP SYSTEM RECORDER, MODEL PMU800
BLACKROCK NEUROPORT BIOPOTENTIAL SIGNAL PROCESSING SYSTEM
NEUROMETRIX BIOAMPLIFIER
PORTI 7 PHYSIOLOGICAL AMPLIFIER
REFA, PHYSIOLOGICAL AMPLIFIER
G.USBAMP
BE PLUS / AURA-LTM64 AMPLIFIER
SINGLE AMPLIFIER FOR BOTOX
OPTI-AMP DC-POWERED
NIC36 AMPLIFIER
SANDMAN SD20 AMPLIFIER
MIZAR, BASIS BE, SANDMAN DIGITAL
SENSOR AMPLIFIER
GRASS MODEL 15 NEURODATA AMPLIFIER SYSTEM
MMC AMPLIFIER
OPTI-AMP
AM-PAK
THE WONDER BOX
VISTA GRAPH POLYSOMNOGRAPHY AMPLIFIER
MULTI-CHANNEL ISOLATION AMPLIFIER (MCIA)
AMPLAID EMG15
MODEL MEB-5304 EVOKED POTENTIAL & ELECTRO. RECORD
THE VENUS SYSTEM
MEM-4104 EVOKED RESPONSE/ELECTROMYOGRAPHY RECORDER
NICOLET AMP 6R11 SYSTEM
PHD-36 PHYSIOLOGICAL SIGNAL AMPLIFIER
AMPLAID MK15 (EVOKED POTENTIAL SYSTEM)
NEUROPACK II 5100
COMPUTERSCOPE CPS-ABR
METRACO EVOKED POTENTIAL SYSTEM
RESPONSE SYSTEM, TN-3000

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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