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: QVR FDA class 2

Multiplex Nucleic Acid Detection System For Biothreat Agents

Immunology

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The Multiplex Nucleic Acid Detection System for Biothreat Agents is a qualitative in vitro diagnostic test designed to simultaneously detect and identify nucleic acids from multiple biothreat pathogens in human clinical specimens, supporting rapid laboratory response to potential bioterrorism or public health emergency events. Classified as FDA Class 2 under regulation 866.4000, it requires 510(k) clearance in the Immunology specialty with review by the Microbiology panel. It is not an implant and not life-sustaining.

510(k) Clearances

2 matches
K Number
Device Name
T2 Biothreat Panel
BioFire Global Fever Special Pathogens Panel; BIOFIRE SHIELD Control Kit for the BioFire Global Fever Special Pathogens Panel

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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