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: QAA FDA class 2

Coccidioides Spp. Nucleic Acid Detection System For Respiratory Specimens

Microbiology

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The Coccidioides spp. Nucleic Acid Detection System for Respiratory Specimens is a qualitative in vitro diagnostic test for the detection of Coccidioides spp. nucleic acids directly in clinical respiratory specimens from patients with signs and symptoms of coccidioidomycosis (Valley fever) and suspicion of infection. It is classified as a Class 2 device under regulation 866.3376, requiring 510(k) premarket notification, and falls within the Microbiology (MI) medical specialty. The product code is QAA. It is not an implant and is not life-sustaining.

510(k) Clearances

1 matches
K Number
Device Name
GeneSTAT.MDx Coccidioides 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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