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.

Product Code: DIR FDA class 2

Free Radical Assay, Cocaine

Clinical Toxicology

View full classification →

The Free Radical Assay for Cocaine is a laboratory method that uses free radical chemistry to detect and quantify cocaine in biological specimens, supporting forensic and clinical toxicology investigations. It is classified as FDA Class 2, requiring 510(k) premarket notification, and is regulated under 21 CFR 862.3250 within the Clinical Toxicology specialty. The device is eligible for third-party 510(k) review.

510(k) Clearances

1 matches
K Number
Device Name
DU PONT PHENYTOIN ASSAY AND CALIBRATOR

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