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: HKO FDA class 1

Refractometer, Ophthalmic

Ophthalmic

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The Ophthalmic Refractometer is an instrument used to measure the refractive index of ocular fluids or to objectively determine refractive error of the eye, aiding in the diagnosis of conditions such as myopia, hyperopia, and astigmatism. It is classified as FDA Class 1, the lowest risk category, subject only to general controls without a premarket notification requirement. The product code is HKO, regulated under 21 CFR 886.1760, within the Ophthalmic medical specialty. No special risk flags apply to this device.

510(k) Clearances

35 matches
K Number
Device Name
TOPCON MODEL BV-1000 AUTOMATED SUBJECTIVE REFRACTION SYSTEM
WAVESCAN WAVEFRONT SYSTEM MODEL HS 1
DIGITAL RETINOSCOPIC PHOTOMETER
VIDEO VISION ANALYZER (VIVA), VRB 100
AUTO REF-KERATOMETER, RK-3
AUTO REFF-30
AUTOREF LENSMETER RL-10
OPTEC 3000
BURTON AUTO REFRACTOR/KERATOMETER - MODEL BARK-8
BURTON AUTO REFRACTOR - MODEL BAR-7
OPTEC 2300 AFVT, ARMED FORCES VISION TESTER
AR-1600G AUTO-REFRACTOMETER
SHIN NIPPON AUTO REFRACTOMETER QR-007N
NIDEK RT-1200S (MARCO TRS-1200)
NIDEK AR-1200
CANON AUTOREFRACTOMETER R-22
CANON AUTOREFRACTOMETER R-20
NIDEK ARK-2000
ALLERGAN HUMPHREY AUTO-REFRACTOR, MODELS 525 & 540
BAUSCH & LOMB GR-3 REFRACTOR
AR-1100 AUTOMATIC REFRACTOR
AR-1600 AUTOMATIC REFRACTOR
AR-1000 AUTOMATIC REFRACTOR
VISION TESTER
CANON AUTOREF R-10
AUTO REFRACTOMETER
AUTOMATIC OBJECTIVE REFRACTOR 2000
I.V.E. REFRACTION SYSTEM
SR-1V DATA PRINTER
AUTO REFRACTOMETER NR-1000
SR-IV PROGRAMMED SUBJECTIVE REFRACTOR
OBJECTIVE REFRACTOR
DIOPTRON III AUTOREFRACTOR
AUTOREFRACTOR, SUBJECTIVE
SUBJECTIVE REFRACTOR, MOSEL SR-111

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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