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: GWN FDA class 2

Nystagmograph

Neurology

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The Nystagmograph is a neurological diagnostic device used to detect, record, and analyze nystagmus (involuntary eye movements) to evaluate vestibular and central nervous system function, aiding in the diagnosis of disorders affecting balance and coordination. It is classified as FDA Class 2, presenting moderate risk and requiring 510(k) premarket clearance. The product code is GWN, regulated under 21 CFR 882.1460 in the Neurology specialty. This device is eligible for third-party 510(k) review.

510(k) Clearances

50+ matches
K Number
Device Name
ICS Dizcovery (1091)
Synapsys VHIT
NeuroSwift Pro
Insight Infrared Video Goggles
VisualEyes
I-Portal Neuro Otologic Test Center, I-Portal Video Nystagmography System, I-Portal Portable Assessment System - Nysragmograph
RightEye Vision System
DizzyDoctor System 1.0.0
I-Portal Neuro Otologic Test Center; I-Portal Video Nystagmography System; I-Portal Video Oculography Eye Tracking System
I-Portal Portable Assessment System - Nystagmograph (I-PAS)
ISEN-Goggles with Data Viewer
VisualEyes
Synapsys Ulmer Video Nystagmograph
ISEN-Goggles
EYE-SYNC
VisualEyes
ICS Impulse
I-Portal NOTC, VNG and VOG
EYESEECAM VHIT
NYSTAGRAM VIDEO NYSTAGMOGRAPHY SYSTEM
ICS IMPULSE
I-PORTAL 4D VIDEO OCULOGRAPHY EYE TRACKING SYSTEM (VOG), I-PORTAL VIDEO NYSTAGMOGRAPHY SYSTEM (VNG), I-PORTAL NEURO OTOL
VN415M, VN415B, VO425M, V0425B, 2D-VOG GOGGLES, 2D-VOG SYSTEM
EYETRACKER/IDEAS
BALANCEBACK MOBILE INTUITIVE VNG SYSTEM
CHRONOS VISION EYE TRACKING DEVICE (C-ETD)
FOCUS VNG/ENG TYPE 1068
DDAT OMT
BALANCEBACK VNG SYSTEM
ICS MEDICAL MODEL VG-30 VIDEO GOGGLES
ENGPLUS
EYETECT TREMOR MONITOR UNIT (TMU)
EXPRESSEYE
EYE TRAK TM, COMPUTERIZED ELECTRONYSTAGMOGRAPH (ENG), MODEL ETV-XXXX
ICS MEDICAL CHARTR ENG/VNG DIAGNOSTIC SYSTEM
ULMER (VNG) VIDEO NYSTAGMOGRAPH
ICS MEDICAL VEMR VIDEO EYE MOVEMENT RECORDER
2D VOG - VIDEO-OCULOGRAPHY
VISUALEYES: VIDEO EYE MONITOR
VIDEO EYE TRAKKER
VARIOUS ELECTRODES
INFRARED EYE MOVEMENT MONITOR
HOUSE INFRARED/VIDEO ELECTRONYSTAGMOGRAPH SYSTEM
JANUS ATAC ENG ANALYSIS SYSTEM
NICOLET NYSTAR PLUS SYSTEM
VESTIBULAR AUTOROTATION TEST
COMPUTER EYE TRACKING SYS./ENG EXAM. CHAIR & TABLE
ELECTROCARDIOGRAPH CONTINUOUS MONITOR
NYSTAGMOGRAPH EOG/ENG ANALYSES
ELECTRONYSTAGMOGRAPH (ENG RECORDER)

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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