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: JJP FDA class 1

Electrode, Ion Selective (Non-Specified)

Clinical Chemistry

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This device is a non-specified ion-selective electrode used in clinical chemistry analyzers to measure the concentration of specific ions in patient specimens, serving as a component within broader analytical systems for electrolyte and metabolite testing. It is classified as FDA Class 1 and is exempt from Good Manufacturing Practice (GMP) requirements, reflecting its low regulatory burden. The product code is JJP, regulated under 21 CFR 862.2050, within the Clinical Chemistry medical specialty.

510(k) Clearances

3 matches
K Number
Device Name
CENTRIPREP 100
NOVA II SODIUM/POTASSIUM/LITHIUM ANALYZER
URINE DILUENT-FOR USE WITH ION SELECTIVE ELECTRODE

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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