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: HME FDA class 1

Chair, Ophthalmic, Ac-Powered

Ophthalmic

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The AC-Powered Ophthalmic Chair is an electrically powered examination chair used in ophthalmic clinical settings, offering motorized positioning adjustments to accommodate patients of varying size and mobility during comprehensive eye examinations. It is classified as FDA Class 1, the lowest risk level, subject only to general controls without a premarket notification requirement. The product code is HME, regulated under 21 CFR 886.1140, within the Ophthalmic medical specialty. No special risk flags apply to this device.

510(k) Clearances

16 matches
K Number
Device Name
MARCO, MARCOTILT, ENCORE AND CUSTOM CHAIR
BREATH-EASY, MODIFICATION
RELIANCE(R) 6200 EXAMINATION CHAIR
STORZ ENT/OPHTHALMIC MAXI CHAIR
MODEL 6500 OPTHALMIC CHAIR
MAC 150E OPTHALMIC CHAIR
THE ERGOSYSTEM CHAIR
-OM WEST 2000 GNATUS CHAIR
TECHNA VISION, INC. ELECTRIC CHAIR
RELIANCE 6100
RELIANCE 5000
RELIANCE 1000, RELIANCE 1500, RELIANCE 2000
WOODLYN CLASSIC EXAM. CHAIR
DOWING OPHTHALMIC CHAIR AC-POWERED
A O CUSTOM II CHAIR AND STAND
MAXI-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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