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: IXX FDA class 2

Processor, Cine Film

Radiology

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A cine film processor is an automatic processing device specifically designed to develop cine radiographic film, such as that used in cardiac catheterization and angiography procedures, where images are captured at high frame rates on motion picture film. It is classified as FDA Class 2, indicating moderate risk and requiring 510(k) premarket notification. The product code is IXX, regulated under 21 CFR 892.1900, within the Radiology medical specialty.

510(k) Clearances

6 matches
K Number
Device Name
JAMIESON MODEL 2100 CINE FILM PROCESSOR AND KODAK CINEFLURE PROCESSOR MODEL 2100
AP-6CR CINERADIOGRAPHIC FILM PROCESSOR
JAMIESON JT-CRP CINE FILM PROCESSOR
STERILE O. R. TOWEL
CINE RADIOGRAPHIC FILM PROCESSOR M-45CR
RADIOGRAPHIC FILM PROCESSOR M-30CR &

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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