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.

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Describe your device and the Research Assistant searches 510(k)s, compares intended use, and drafts a predicate shortlist — with citations.

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Product Code: IXL FDA class 2

Device, Spot-Film

Radiology

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A spot-film device is an accessory component used with fluoroscopic systems to enable rapid acquisition of radiographic spot images during fluoroscopic examinations, allowing the capture of static images at selected moments during dynamic studies. It is classified as FDA Class 2, indicating moderate risk and requiring 510(k) premarket notification. The product code is IXL, regulated under 21 CFR 892.1670, within the Radiology medical specialty.

510(k) Clearances

13 matches
K Number
Device Name
OPTIMA XR120
MD-1835
ADVANTX 1824 SPOTFILM DEVICE
KODAK AUTOMIXER III INTEGRATED, KODAK AUTOMIXER III 180 LP
AXT 1400 SPOTFILM DEVICE
DIAGNOST 76 FAMILY*R/F SYSTEMS - RELEASE 4.4
ELITE R/F SPOT FILM DRIVE
SFD-035 SPOT FILM DEVICE
A.X.T. SPOTFILM DEVICE
14X14 MULTIFORMAT SPOT FILMER, NO. 6650.400
SPOT-FILM DEVICE 8835
RAYTHEON MEDICAL IMAGING
MULTI-FORMAT SFD MODEL 1720

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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