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.

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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: QEF FDA class 1

Pressure Ulcer Management Tool

Gastroenterology, Urology

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The Pressure Ulcer Management Tool is a prescription device intended for patients at risk of developing pressure ulcers, providing output that supports a user's decision to increase intervention; it is an adjunct tool for pressure ulcer management and is not intended for detection or diagnostic purposes. It is classified as FDA Class 1, with no premarket notification required, under regulation 876.2100 in the Gastroenterology and Urology specialty. The product code is QEF. It is not an implant and is not life-sustaining.

510(k) Clearances

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SEM Scanner (Model 200)

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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