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: MLM FDA class 2

Enzyme Immunoassay, Tracrolimus

Clinical Chemistry

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The Enzyme Immunoassay for Tacrolimus is an in vitro diagnostic device used to measure tacrolimus (FK506) concentrations in patient whole blood to support therapeutic drug monitoring in solid organ transplant recipients, where maintaining appropriate drug levels is critical to preventing graft rejection while minimizing drug toxicity. Classified as a Class 2 device under 21 CFR 862.1678 within the Clinical Chemistry specialty, it requires 510(k) premarket notification. It carries no implant or life-sustaining flags.

510(k) Clearances

9 matches
K Number
Device Name
Tacrolimus Assay Kit
Elecsys Tacrolimus
Dimension Tacrolimus Flex® Reagent Cartridge (TAC), Dimension Tacrolimus Calibrator (TAC CAL)
THERMO SCIENTIFIC QMS TACROLIMUS ASSAY AND CALIBRATORS
ARCHITECT TACROLIMUS: MODEL 1L77
MASSTRAK IMMUNOSUPPRESSANTS KIT
DIMENSION TACR FLEX REAGENT CARTRIDGE, MODEL DF107
EMIT 2000 TACROLIMUS ASSAY AND SAMPLE PRETREATMENT REAGENT
CEDIA TACROLIMUS ASSAY

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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