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510(k) Data Aggregation

    K Number
    K033637
    Manufacturer
    Date Cleared
    2003-12-17

    (28 days)

    Product Code
    Regulation Number
    892.2030
    Reference & Predicate Devices
    N/A
    Why did this record match?
    Device Name :

    MEDICAL IMAGE DIGITIZER, MODEL 2908

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
    Intended Use

    Model 2908 is an image scanner which reads black and white images from transmitted light through an X-ray film and the like, and transfers the images, as the digital data, to a computer.

    This device has no patient contacting materials and is intended to be used by trained personnel only.

    The output of the device is to be evaluated by additionally trained personnel capable of sufficient review to afford identification and intervention In case of malfunction.

    Device Description

    Model 2908 is an image scanner which reads black and white images from transmitted light through an X-ray film and the like, and transfers the images, as the digital data, to a computer.

    AI/ML Overview

    The provided document is a 510(k) clearance letter from the FDA for a medical image digitizer (Film Digitizer, Model 2908). This document grants market clearance for a device based on its substantial equivalence to a predicate device. It does not contain any information regarding acceptance criteria, study details, or device performance against specific metrics.

    Therefore, I cannot fulfill the request for a table of acceptance criteria and reported device performance, nor can I provide information about sample sizes, ground truth establishment, expert qualifications, adjudication methods, MRMC studies, or standalone performance. The document focuses on regulatory approval rather than technical performance validation.

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