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: JZJ FDA class 1

Prealbumin, Antigen, Antiserum, Control

Immunology

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Prealbumin, Antigen, Antiserum, Control is an immunological reagent set used to measure prealbumin (transthyretin) concentrations in serum, serving as a sensitive indicator of nutritional status and hepatic protein synthesis, and used in the evaluation of malnutrition and hepatic disease. It is classified as FDA Class 1, the lowest risk category, subject to general controls only. The product code is JZJ, regulated under 21 CFR 866.5060, and falls within the Immunology medical specialty.

510(k) Clearances

11 matches
K Number
Device Name
RANDOX PREALBUMIN
TINA-QUANT PREALBUMIN
HUMAN PREALBUMIN RADIAL IMMUNODIFFUSION KIT
PREALBUMIN IMMUNOLOGICAL NL TEST KIT
SPQ(TM) TEST SYSTEM FOR PREALBUMIN
SPQ(TM) TEST SYSTEM FOR MICROALBUMIN
QM300 PREALBUMIN ANTIBODY PACK
ANTISERUM TO HUMAN PREALBUMIN
LASER PREALBUMIN TEST
PREALBUMIN ENZYME IMMUNOASSAY
LAS-R HUMAN PREALBUMIN TEST

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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