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: HMF FDA class 1

Stand, Instrument, Ac-Powered, Ophthalmic

Ophthalmic

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The AC-Powered Ophthalmic Instrument Stand is an electrically powered support stand used to hold and position ophthalmic diagnostic equipment such as slit lamps, refractors, and tonometers at the appropriate height and angle during patient examinations. It is classified as FDA Class 1, the lowest risk category, requiring only general controls without a premarket notification. The product code is HMF, regulated under 21 CFR 886.1860, within the Ophthalmic medical specialty. No special risk flags apply to this device.

510(k) Clearances

15 matches
K Number
Device Name
ROTA SYSTEM 5000
ROTA DATAMATE I
ROTA SYSTEM XL
MARCO INTERNATIONAL STAND
BURTON OPHTHALMIC STAND - MODEL XL3200
BURTON OPHTHALMIC EXAM UNIT - MODEL 2201
OPHTHALMIC STAND
RELIANCE PENDULUM OPHTHALMIC DELIVERY SYSTEM
OPHTHALMIC CHAIR
OPHTHALMIC STAND
ELECTRIC INSTRUMENT TABLE
RELIANCE OPHTHALMIC INSTRUMENT CONTROL
SYSTEM 1 INSTRUMENT STAND
B & L OPHTHALMIC INSTRUMENT STAND
B & L OPHTHALMIC CHAIR

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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