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: QYT FDA class 2

Over-The-Counter Covid-19 Antigen Test

Microbiology

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The over-the-counter COVID-19 antigen test (product code QYT) is a Class 2 Microbiology in vitro diagnostic device (regulation 866.3984) intended for the rapid, qualitative detection of SARS-CoV-2 virus nucleocapsid protein antigen in individuals 2 years and older. It requires 510(k) clearance and is designed for non-prescription consumer use. It is not an implant and is not life-sustaining.

510(k) Clearances

14 matches
K Number
Device Name
Fastep COVID-19 Antigen Pen Home Test; Fastep COVID-19 Antigen Pen Test
Heal-Check Rapid COVID-19 Antigen Self-Test
GenBody COVID-19 Ag Home Test
COVID-19 Detect Rapid Self -Test
GenaCheck COVID-19 Rapid Self-Test
OHC COVID-19 Antigen Self Test
BinaxNOW™ COVID-19 Antigen Self Test
CareSuperb™ COVID-19 Antigen Home Test
Wondfo 2019-nCoV Antigen Test (Lateral Flow Method)
CorDx Tyfast COVID-19 Ag Rapid Test; CorDx COVID-19 Ag Test
iHealth COVID-19 Antigen Rapid Test
Flowflex® Plus COVID-19 Home Test
QuickVue COVID-19 Test
Flowflex COVID-19 Antigen Home 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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