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: HOW FDA class 1

Drum, Opticokinetic

Ophthalmic

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An Optokinetic Drum is a diagnostic ophthalmic instrument consisting of a rotating cylinder with alternating stripes used to elicit optokinetic nystagmus, a reflexive eye movement, for assessing visual acuity in non-verbal patients and evaluating afferent visual pathway integrity. This device is FDA Class 1 (lowest risk), requiring only general controls without premarket notification. It carries product code HOW and is regulated under 21 CFR 886.1200, within the Ophthalmic medical specialty. It is exempt from Good Manufacturing Practice (GMP) requirements.

510(k) Clearances

1 matches
K Number
Device Name
MODEL 5400 OPTOKINETIC STIMULATOR

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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