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: KKH FDA class 1

Tablet, Resazurin

Hematology

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The Resazurin Tablet is a redox indicator reagent used in hematology and microbiology laboratory procedures, applied as a colorimetric indicator to assess cell viability and metabolic activity in biological samples. It is classified as FDA Class 1, indicating low risk subject to general controls without a requirement for premarket clearance or approval. The product code is KKH and the applicable regulation is 21 CFR 864.1850 under the Hematology specialty. This device is GMP exempt.

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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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