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: QAT FDA class 2

Brain Trauma Assessment Test

Immunology

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The Brain Trauma Assessment Test is an in vitro diagnostic device intended as an aid in the evaluation of patients with suspected mild traumatic brain injury (TBI), used in conjunction with other clinical information to assist in determining the need for radiologic head imaging per current standard of care. It is classified as a Class 2 device under regulation 866.5830, requiring 510(k) premarket notification and eligible for third-party review, falling within the Immunology (IM) medical specialty. The product code is QAT. It is not an implant and is not life-sustaining.

510(k) Clearances

6 matches
K Number
Device Name
VIDAS TBI (GFAP, UCH-L1)
i-STAT TBI Cartridge with the i-STAT Alinity System
TBI
Traumatic brain injury (TBI) test
i-STAT TBI Plasma cartridge with the i-STAT Alinity System
Banyan BTI

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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