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: HPT FDA class 1

Perimeter, Automatic, Ac-Powered

Ophthalmic

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An Automatic AC-Powered Perimeter is an electrically powered ophthalmic diagnostic device that automatically presents light stimuli at predetermined or algorithmically selected locations across the visual field and records patient responses, providing standardized and efficient mapping of visual field defects. This device is FDA Class 1 (lowest risk), subject to general controls without requiring premarket notification. It carries product code HPT and is regulated under 21 CFR 886.1605, within the Ophthalmic medical specialty.

510(k) Clearances

41 matches
K Number
Device Name
MAIA, MODEL 1
GUIDED PROGRESSION ANALYSIS ON THE HUMPHREY FIELD ANALYZER II AND II -I SERIES
FORESEE HOME
TRUEFIELD ANALYZER
THE NOTAL VISION PREVIEW PREFERENTIAL HYPERACUITY PERIMETER (PREVIEW PHP)
NOVAVISION, MODEL 2.0
KASHA VISUAL FIELD SYSTEM
AUTOMATIC VISUAL FIELD PLOTTER AP-125
HUMPHREY FIELD ANALYZER (HFA II)
FIELD TREND
MS-30 AUTOMATIC PERIMETER
OPTICOM M600
LD 400
PERIKON PCL 90
MT-336 AUTOMATIC PERIMETER
OPTIFIELD I AND II AUTOMATED PERIMETERS
OPTIMED ADVANTAGE
AUTOMATIC PERIMETER, AP-340
PATTERN DISCRIMINATION PERIMETER
TKS 4000 AUTO PERIMETER
DIGILAB MODEL 1500 PERIMETER
TECHNA VISION AUTO-PERIMETER
THE FIELDMASTER MODEL 275
HUMPHREY FIELD ANALYZER MODEL 630
DIGILAB 750 AUTOMATED PERIMETER W/IBM PERSON/COMPU
QUANTUM 412
OCTOPUS 500/500E
OCUMAP 100 AUTOPERIMETER
DIGILAB 350 THE KRAKAU PERIMETER
DICON GLAUCOMA DIAG. CENTER 2000 SERIES
MODEL 200 SQUID
FIXATION MONITOR
AUTO PERIOMETER 3000
THE HUMPHREY FIELD ANALYZER MODEL 610
DICON AUTO PERIMETER 200
DICON AUTO PERIMETER 2000
AUTOMATED PERIMETERS
AUTO-FIELD D AUTOMATED VISUAL DETECTOR
BAYLOR VISUAL FIELDS PROGRAMMER
AUTO-FIELD II OPHTHALMIC FIELD SCANNER
OCTOPUS

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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