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: IWZ FDA class 1

Film, Radiographic

Radiology

View full classification →

Radiographic film is a photosensitive medium used to capture and store X-ray images, consisting of a base material coated with a silver halide emulsion that responds to ionizing radiation to produce a latent image which is then chemically processed. It is classified as FDA Class 1, the lowest risk category, subject only to general controls. The product code is IWZ, regulated under 21 CFR 892.1840, within the Radiology medical specialty.

510(k) Clearances

34 matches
K Number
Device Name
KODAK EKTASIAN HG FILM (EHG-15)
VOXGRAM
3M MEDICAL DIAGNOSTIC VIDEOCASSETTE
3M MEDICAL DIAGNOSTIC SUPER VHS VIDEOCASSETTE
ORWO X-RAY FILM
KODAK DENTAL BARRIER PAC
KODAK CFT FILM SO-141
TYPE 633 COMPUTED RADIOGRAPHY (CR) FILM
MEDICAL X-RAY FILM
BELMONT AUTOPAN-PANORAMIC 098 CEPHALOMETRIC-RADIOG
FR MEDICAL X-RAY FILM
POWERMAT VRP-1 X-RAY IMAGING
WILCOR-XR RP-L MEDICAL FILM
WILCOR-XR RP MEDICAL FILM
WILCOR-XR RP-OG MEDICAL FILM
SINGUL-XR RP NON SCREEN MED. FILM
KODAK T-MAT L FILM SO-387
CRONEX LO-DOSE MAMMOGRAPHY
KODAK CINEFLUOROGRAPHIC FILM SO-274
POLAROID TPX RADIOGRAPHIC FILM
KODAK ORTHO L FILM
KODAK EKTASPEED DENTAL X-RAY FILM
HOPE MODEL 126, AUTO/PROCES., DEN. FLM
KODAK X-OMAT M20 PROCESSOR, MODEL 1
KODAK ORTHO G FILM
KODAK X-OMAT G FILM
KODAK CFN FILM SO-224
SR 301 MEDICAL X-RAY FILM
KODAK X-OMAT M20 PROCESSOR, MODEL 2
KODAK X-OMAT RP FILM
KODAK ORTHO M FILM
KODAK GRAY TONE IMAGING FILM
ORTHO H FILM
GRAY TONE IMAGING FILM

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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