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: LCC FDA class 2

Applicator, Ocular Pressure

Ophthalmic

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An ocular pressure applicator is an ophthalmic instrument used to apply controlled pressure to the eye, typically to facilitate intraocular lens implantation, reduce intraocular pressure, or assist in other ophthalmic surgical or diagnostic procedures. It is classified as FDA Class 2, requiring 510(k) premarket notification. The product code is LCC, regulated under 21 CFR 886.4610, in the Ophthalmic specialty. Third-party review eligibility applies.

510(k) Clearances

6 matches
K Number
Device Name
ILWAIT TIMER OCULOPRESSOR
WEE BAG O'MERCURY
OCULAR PRESSURE REDUCER (MCCANNEL)
WEE BAG O'MERCURY
RELIEF VALVE-HONAN INTRAOC. PRESSURE
NEVYAS AUTOPRESS EYE COMPRESSOR

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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