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: IXC FDA class 1

Illuminator, Radiographic-Film

Radiology

View full classification →

A radiographic film illuminator, also known as a viewbox or negatoscope, is a device that provides uniform backlighting to enable diagnostic interpretation of radiographic films by clinicians in a darkened or subdued light environment. It is classified as FDA Class 1, the lowest risk category, subject only to general controls. The product code is IXC, regulated under 21 CFR 892.1890, within the Radiology medical specialty.

510(k) Clearances

18 matches
K Number
Device Name
SMARTLIGHT DIGITAL FILM VIEWER, MODELS SL 4000PLUS, SL 2000PLUS
SMART MOTORIZED VIEWER
ARRIPRO 35 ST/TV
DIFFUSER PANEL
LILY DARK VIEWER
VOXBOX
ADVIEWER 2000
ULTRALITE X-RAY FILM ILLUMINATOR
ROTOLUX, SELECTOLUX, SHUTTERVUE
EXCELVIEW ILLUMINATOR
VARIVIEWER (X-RAY FILM VIEWER)
PROVIEW (E7015) & PROLINK IMAGE DISPLAY SYSTEM
SANDHILL ELECTRONIC CALIPER
LF MOTORIZED RADIOGRAPHIC FILM VIEWER
MEDI VIEW
VIEW-LITE, MODEL-SL
VIEW-LITE, MODEL-S
VIEW-LITE, MODEL-DL

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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