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: NOP FDA class 2

Elisa, Antibody, West Nile Virus

Microbiology

View full classification →

The West Nile Virus ELISA antibody test is a microbiology diagnostic device intended for the detection of IgG and IgM antibodies to West Nile Virus in serum or cerebrospinal fluid from symptomatic patients. It is classified as FDA Class 2 under regulation 866.3940 in the Microbiology specialty, requiring 510(k) premarket notification to demonstrate substantial equivalence. Product code NOP is not eligible for third-party review and is not an implant or life-sustaining device.

510(k) Clearances

10 matches
K Number
Device Name
EUROIMMUN Anti-West Nile Virus ELISA (IgM)
EUROIMMUN Anti-West Nile Virus ELISA (IgG)
SPECTRAL WEST NILE VIRUS IGM STATUS TEST
WEST NILE DETECT IGM ELISA
WEST NILE VIRUS IGG INDIRECT ELISA
WEST NILE VIRUS IGM CAPTURE ELISA, MODEL E-WNV02M
WEST NILE VIRUS IGM CAPTURE ELISA
WEST NILE VIRUS IGM CAPTURE ELISA, MODEL EL0300M
WEST NILE VIRUS ELISA IGG, MODEL EL0300G
WEST NILE VIRUS IGM CAPTURE ELISA

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.

Popular Product Codes

Commonly searched