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: JZW FDA class 1

Nephelometer

Immunology

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A nephelometer is a laboratory instrument used to measure the turbidity or light-scattering properties of a solution, commonly employed in immunology testing to quantify proteins, antibodies, and other analytes in serum or other body fluids. It is regulated as an FDA Class 1 device, the lowest risk category, meaning it is subject only to general controls such as proper labeling and manufacturing standards, with no requirement for premarket notification. The product code is JZW, regulated under 21 CFR 866.4540, within the Immunology medical specialty. No special flags apply to this device.

510(k) Clearances

11 matches
K Number
Device Name
BN PROSPEC SYSTEM
BEHRING LASER NEPHELOMETER
BEHRING NEPHELOMETER 100
RRT SYSTEM LASER REFLECTOMETER ANALYZER
TURBOX
BCM-302 COLLIMATING CONE & COMPENSATIN
DISC 120 TRANSPORTER
LANCER L-INA BUFFER, POLYMER, WASH SOLU
IMMUNOCHEMISTRY SYS. MANUAL MODE
ANTISERUM HUMAN (PRO.) NEPHELOMETRIC GR.
LASER STANDARD SERUM

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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