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.

Let the assistant find your predicates

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: HMY FDA class 1

Keratome, Battery-Powered

Ophthalmic

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The Battery-Powered Keratome is a portable, battery-operated surgical instrument used to make precise incisions in the cornea during ophthalmic procedures such as cataract surgery or corneal transplantation. It is classified as FDA Class 1, the lowest risk category, and requires 510(k) premarket notification before marketing, demonstrating substantial equivalence to a predicate device. The product code is HMY, regulated under 21 CFR 886.4370, within the Ophthalmic medical specialty. This device is eligible for third-party 510(k) review by an FDA-accredited reviewer.

510(k) Clearances

12 matches
K Number
Device Name
ONEUSE- PLUS MICROKERATOME
BD K-4000 MICROKERATOME SYSTEM
BD-3000 MICROKERATOME SYSTEM, MODEL K-3000 MICROKERATOME
M2 SINGLE USE MICROKERTOME
CARRIAZO BARRAQUER SINGLE USE MICROKERATOME
CARRIAZO BARRAQUER II MICROKERATOME
MILLENIUM MICROKERATOME, MODEL IMD-001
KERATOME SYSTEM, MODEL K3000
CARRIAZO BARRAQUER MICROKERATOME
KERATOME SYSTEM
VISI-DRAPE OPHTHALMIC DRAPES
OSCILLATING KNIFE AND ACCESSORIES

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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