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: QXA FDA class 2

Lateral Flow Immunochromatography Assay For Host Biomarkers Of Respiratory Infection

Microbiology

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The lateral flow immunochromatography assay for host biomarkers of respiratory infection (product code QXA) is a Class 2 Microbiology in vitro diagnostic device (regulation 866.3230) intended to detect and qualitatively or quantitatively measure one or more non-microbial analytes in human clinical specimens to aid in the assessment or identification of a localized microbial infection when used in conjunction with clinical signs, symptoms, and other laboratory findings. It requires 510(k) clearance. It is not an implant and is not life-sustaining.

510(k) Clearances

2 matches
K Number
Device Name
FebriDx Bacterial/Non-bacterial Assay
FebriDx Bacterial / Non-bacterial Point of Care Assay

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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