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: QYV FDA class 2

Digital Cervical Cytology Slide Imaging System With Artificial Intelligence Algorithm

Pathology

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The digital cervical cytology slide imaging system with artificial intelligence algorithm (product code QYV) is a Class 2 Pathology prescription in vitro diagnostic device (regulation 864.3900) consisting of an automated digital slide creation, viewing, and management system that uses AI and machine learning to analyze digital images of Pap test specimens and conventional Pap smears, selecting and presenting areas of interest to facilitate cytological interpretation and aid in rendering a cytology diagnosis. It requires 510(k) clearance. It is not an implant and is not life-sustaining.

510(k) Clearances

1 matches
K Number
Device Name
“Genius™ Digital Diagnostics System with the Genius™ Cervical AI algorithm”

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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