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.

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Describe your device and the Research Assistant searches 510(k)s, compares intended use, and drafts a predicate shortlist — with citations.

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Product Code: HLX FDA class 2

Photostimulator, Ac-Powered

Ophthalmic

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The AC-Powered Photostimulator is an electrically powered device used in ophthalmic electrophysiology to deliver precisely controlled flashes of light to the retina, eliciting visual evoked potentials or electroretinographic responses for assessment of retinal and visual pathway function. It is classified as FDA Class 2, indicating moderate risk, and requires 510(k) premarket clearance before marketing in the United States. The product code is HLX, regulated under 21 CFR 886.1630, within the Ophthalmic medical specialty. This device is eligible for third-party 510(k) review by an FDA-accredited reviewer.

510(k) Clearances

18 matches
K Number
Device Name
MODIFICATION TO EDI VERIS SYSTEM
EDI VERIS SYSTEM
CLARUS ENDOSCOPIC HOOK KNIFE
RETINA TESTER
SCOPTOPIC SENSITIVITY TEST-1[SST-1]
IRAS EDS INTERFEROMETRIC STIMULATOR
PHOTRON NEUROVISUAL STIMULATOR(MODIFICATION)
DOWNING SPECTRAL ILLUMINATOR
MILLER/NADLER GLARE TESTER
LED GOGGLES
CONTRAST SENSITIVITY EQUIPMENT
5031 BRIGHT FLASH STIMULATOR
5012 PARABOLIC STIMULATOR
5010 VISUSTIM
5011 GANZFELD STIMULATOR
VTS-1000 VISUAL TESTING SYSTEM
PANTOPS M-2 ELECTROPHYSIOLOGY SYSTEM
COMPUTERIZED ELECTRO-OCULOGRAPH

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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