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: QYA FDA class 2

System For Detection Of Nucleic Acid From Non-Viral Microorganism(S) Causing Stis Using Specimens Collected At Home

Microbiology

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The system for detection of nucleic acid from non-viral microorganisms causing STIs using specimens collected at home (product code QYA) is a Class 2 Microbiology in vitro diagnostic device (regulation 866.3385) intended for self-collection of specimens in home settings, with subsequent laboratory testing for detection of nucleic acids from non-viral sexually transmitted infection pathogens to aid in diagnosis. It requires 510(k) clearance and may be used for prescription or over-the-counter purposes. It is not an implant and is not life-sustaining.

510(k) Clearances

2 matches
K Number
Device Name
simpli-COLLECT STI Test
Simple 2 Test

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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