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: IXW FDA class 2

Processor, Radiographic-Film, Automatic

Radiology

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An automatic radiographic film processor is a device that mechanically transports radiographic film through chemical developer, fixer, wash, and drying stages to produce a developed radiographic image, replacing manual darkroom processing. It is classified as FDA Class 2, indicating moderate risk and requiring 510(k) premarket notification. The product code is IXW, regulated under 21 CFR 892.1900, within the Radiology medical specialty.

510(k) Clearances

50+ matches
K Number
Device Name
XTENDER FILM PROCESSOR, SPRINT FILM PROCESSOR MODEL XTENDER MODEL SPRINT
INTRAX FILM PROCESSOR
OPTIMAX, COMPACT 2, OPTIMAX 2010, ECOMAX
RADIOGRAPHIC FILM PROCESSOR, MODELS XP400 AND XP1000
FILM PROCESSOR, MODEL LIFE RAY PRO 1000
FILM PROCESSOR, MODEL LIFE RAY PRO 2500
AX200 AUTOMATIC X-RAY FILM PROCESSOR, MODEL 6586.036
LEVEL 356 X-RAY FILM PROCESSOR, MODELS MD & MD-D
FREEDOM AUTOMATIC FILM PROCESSOR
MICRO-MAX, MODEL 319
ALL-PRO 2010
OPTIMAX/ COMPACT 2
KONICA SRX- 701 AUTOMATIC X-RAY FILM PROCESSOR
AII-PRO 100 PLUS AND ALL-PRO 200
CP 1000, CURIX HT 330, CLASSIC E.O.S., CURIX HT 530, MAMORAY HT 300, MAMORAY CMPACT PLUS, CURIX COMPACT PLUS, CURIX COMS
MAMMOLOADER BY C.M.A. SRL
KODAK MINILOADER(2000)
3M TRIMATIC MODULAR ADVANCED PROCESSING SYSTEM AND 3M APS AUTOMATIC FILM PROCESSOR
JPI AUTOMATIC X-RAY FILM PROCESSOR
FUJI COMPUTED RADIOGRAPHY SYSTEM FCR9000HQ, FCR9501HQ
DOOSAN DSP 3800 AUTOMATIC X-RAY FILM PROCESSOR
KODAK AUTOMIXER II PLUS
KODAK X-OMAT 3000 RA PROCESSOR
KODAK X-OMAT 5000 RA PROCESSOR
FUJI COMPUTED RADIOGRAPHY SYSTEMS
JPI AUTOMATIC X-RAY FILM PROCESSOR
X-RAY FILM PROCESSOR
KONICA SRX-201 AUTOMATIC X-RA FILM PROCESSOR
VELO ACE
3M XP-2000 X-RAY FILM PROCESSOR
KODAK X-OMAT M43A, M43, & CLINIC 1 PROCESSORS
FUJI MEDICAL FILM PROCESSOR FPM2800
KONICA SRX-501A AUTOMATIC X-RAY FILM PROCESSOR
KONICA DS-7 AUTOMATIC X-RAY FILM PROCESSOR
KONICA SRX-301 AUTOMATIC X-RAY FILM PROCESSOR
KODAK XML 300 DARKROOM FILM FEEDER
KONICA QX-130APLUS AUTOMATIC X-RAY FILM PROCESSOR
KONICA SRX-101 AUTOMATIC X-RAY FILM PROCESSOR
KONICA QX-70 AUTOMATIC X-RAY FILM PROCESSOR
AX-390SE AUTOMATIC X-RAY FILM PROCESSOR 9586.033
MAMMO-300 AUTOMATIC X-RAY FILM PROCESSOR
FUJI DAYLIGHT CASSETTE MULTI-LOADER
AFP 17 X 4 AUTOMATIC FILM PROCESSOR
KODAK EKTASCAN
AX-700LE AUTOMATIC X-RAY FILM PROCESSOR
DU PONT COMPACT DAYLIGHT SYSTEM II (CDS II)
KODAK X-OMAT FS-1A PROCESSOR
AX-300SE AUTOMATIC X-RAY FILM PROCESSOR, 6586.027
KODAK X-OMAT MODEL 180 LP PROCESSOR
KODAK X-OMAT FIXER MANAGER

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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