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: JJO FDA class 1

Flame Emission Photometer For Clinical Use

Clinical Chemistry

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This device is a flame emission photometer used in clinical laboratories to measure the concentration of specific metal ions, most commonly sodium and potassium, in biological specimens by detecting characteristic light emitted when the sample is introduced into a flame. It is classified as FDA Class 1, the lowest risk category, requiring only general controls without a premarket submission. The product code is JJO, regulated under 21 CFR 862.2540, within the Clinical Chemistry medical specialty.

510(k) Clearances

22 matches
K Number
Device Name
FINNIGAN MAT INCOS 50
OLYMPUS AU 5000 FLAME PHOTOMETER MODULE
ELVI 655 FLAME PHOTOMETER
LITHIUM REAGENT
FLAME PHOTOMETERS
DAILY WASH SOLUTION 5
VOLUME TEST DYE 6
SUPPLIES FOR INSTRUMENTATION LAB FLAME
SDI PREPAX DILUKIT 29-1000
POTASSIUM SODIUM ANALYSIS PRODUCTS
FLAME PHOTOMETER T281-T282-T283
SHABAN #9868 TUBING KIT-9870 STYLET
SHABAN #9850 PUMP WINDINGS-9860 FILTER
SHABAN #9858 ASPIRATOR ASSEMBLE #9862-
SHABAN #9852 CHIMNEY-#9854 SCREEN &
IL 943 FLAME PHOTOMETER
CORNING 480 FLAME PHOTOMETER
MICROFLAME PHOTOMETER
FLAME PHOTOMETER, MODEL 435
FLAME PHOTOMETER, MODEL 455
I.L. MODEL 643 FLAME PHOTOMETER
PROPANE, HIGH PURITY, INSTRUMENT GRADE

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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