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: JQX FDA class 1

Nephelometer, For Clinical Use

Clinical Chemistry

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The Nephelometer, For Clinical Use is a clinical chemistry instrument that measures the turbidity of a solution by detecting the intensity of light scattered at an angle by particles in suspension, used in quantifying proteins, immunoglobulins, complement components, and other analytes through nephelometric immunoassay methods. This device is FDA Class 1, the lowest risk category, requiring only general controls and no premarket notification. It carries product code JQX and is regulated under 21 CFR 862.2700, within the Clinical Chemistry medical specialty.

510(k) Clearances

14 matches
K Number
Device Name
IMMAGE IMMUNOCHEMISTRY SYSTEM
ARRAY(R) 360
QMS(TM) - THEOPHYLLINE
TDX ANALYZER W/NEPHELOMETRY CAROUSEL
A-JUST TURBIDITY METER
ALBUMIN NEPHELOMETRIC ASSAY
J.T. BAKER NEPHELOMETER
BIOVATION NEPHELOMETER
NEPHELOMETER, MIC-2000 LASER
RAD-291
ANTIBIOTIC NEPHELOMETER
NEPHELOMETER
LASER IMMUNONEPHELOMETRIC ANALYZER
TRANSPORTEO MODULE

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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