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.

Let the assistant find your predicates

Describe your device and the Research Assistant searches 510(k)s, compares intended use, and drafts a predicate shortlist — with citations.

Free to try · every answer cites its records

Product Code: OAX FDA class 2

Plasmodium Spp. Detection Reagents

Microbiology

View full classification →

The Plasmodium Spp. Detection Reagents (product code OAX) are in vitro diagnostic reagents used for the detection of Plasmodium species antigens in venous or capillary whole blood, aiding in the diagnosis of human malaria infections and the differential diagnosis of Plasmodium falciparum infections from other less virulent Plasmodium species. It is classified as FDA Class 2, requiring 510(k) clearance, and is regulated under 21 CFR 866.3402 within the Microbiology specialty. The device carries no implant or life-sustaining flags.

510(k) Clearances

1 matches
K Number
Device Name
BINAX NOW MALARIA TEST; MODEL 660-000, 660-XXX

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.

Popular Product Codes

Commonly searched