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: JMA FDA class 1

Acid, Ascorbic, 2,4-Dinitrophenylhydrazine (Spectrophotometric)

Clinical Chemistry

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This device is a spectrophotometric clinical chemistry reagent system using 2,4-dinitrophenylhydrazine to measure ascorbic acid (Vitamin C) in patient specimens, used in the assessment of nutritional status and diagnosis of scurvy or conditions associated with vitamin C deficiency or excess. It is classified as FDA Class 1, the lowest risk tier, requiring only general controls with no premarket submission. The product code is JMA, regulated under 21 CFR 862.1095, within the Clinical Chemistry medical specialty.

510(k) Clearances

3 matches
K Number
Device Name
QUANTIMETRIX C-CLEAR(TM)
HELENA BIOSTRIP A
URITEST 9, INLAB REAGENT STRIPS URINALY

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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