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: HOX FDA class 1

Chart, Visual Acuity

Ophthalmic

View full classification →

A Visual Acuity Chart is a standardized diagnostic ophthalmic device consisting of letters, numbers, or symbols of progressively decreasing size arranged in rows, used by clinicians to measure a patient's distance or near visual acuity as part of a routine eye examination or refraction. This device is FDA Class 1 (lowest risk), subject to general controls only without requiring premarket notification. It carries product code HOX and is regulated under 21 CFR 886.1150, within the Ophthalmic medical specialty. It is exempt from Good Manufacturing Practice (GMP) requirements.

510(k) Clearances

32 matches
K Number
Device Name
CENTRAL VISION ANALYZER MODEL 1000
HEINE LAMBDA 100
OCCU-TECH VISION TEST
PL 20/20 INFANT VISION TESTER
VISUAL CONTRAST SENSITI., POTENTIAL ACUITY&GLARE
PG CONSEN CONTRAST SENSITIVITY TESTING PROGRAM
MCT 8000 (MULTI-VISION CONTRAST TESTER)
VCTS 700S SYSTEM
VCTS 6500 SYSTEM
VCTS MARKETING PROGRAM SYSTEM
ADULT PERCEPTUAL MOTOR PUZZLES (5331-01)
OPTEC 1000 DMV VISION TESTER MODIFY
MENTOR B-VAT(TM) II VIDEO TESTER
'E' CUBE AND 'E' PAD
READING CHARTS-CARDS (DISTANCE AND NEARPOINT)
OPTEC 1000 DMV
CANON AUTO ACUITOMETER CV-10
OPTRONICS CONTRAST ACUITY TESTER
IN-HOME VISION MONITORING KIT
MENTOR BRIGHTNESS ACUITY TESTER
VISTECH VCTS GLARE TESTER
VISTECH VCTS 6000
ERGO DIAGNOSTIC CARD
TESTING VISUAL ACUITY
DOT VISUAL ACVITY TEST 2000
VFS 1000/SCREENING FUNCTION ANALYZER
NIC OPTRONICS CS-2000
MENTOR POTENTIAL ACUITY METER
EYE CHARTS
EYETECH-VISION SCREENING SYSTEM
OPHTHALMIC DRESSING TRAY
BAYLOW VISUAL ACUITY TESTER

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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