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510(k) Data Aggregation

    K Number
    K013608
    Date Cleared
    2001-11-15

    (15 days)

    Product Code
    Regulation Number
    892.1650
    Reference & Predicate Devices
    Why did this record match?
    Device Name :

    DIGITAL RADIOGRAPHY SYSTEM, MODEL DFP-8000D

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

    The Digital Radiography System, Model DFP-8000D is a Digital Radiography Processor used in diagnostic X-ray angiography systems. This system processes, displays, and records digital images obtained from the detectors of X-ray TV systems (such as CCD cameras), and replays the recorded images for image diagnosis. This system is intended for use in diagnostic and interventional procedures for cardiac blood vessels, cerebral blood vessels, abdominal blood vessels, and lower limb blood vessels.

    Device Description

    The Digital Radiography System, Model DFP-8000D is a Digital Radiography Processor used in diagnostic X-ray angiography systems. This system processes, displays, and records digital images obtained from the detectors of X-ray TV systems (such as CCD cameras), and replays the recorded images.

    AI/ML Overview

    The provided text is a 510(k) summary for the Toshiba Digital Radiography System, Model DFP-8000D. It describes the device, its intended use, and its technological characteristics in comparison to a predicate device.

    However, the provided document does not contain any information regarding acceptance criteria, study details, performance metrics, sample sizes for training or testing, ground truth establishment, expert qualifications, or adjudication methods.

    The document is a regulatory submission summary that indicates the device received substantial equivalence to a predicate device, which allows it to be marketed. This type of submission typically focuses on demonstrating similarity to an already cleared device, rather than providing detailed performance studies with acceptance criteria as one would find for a novel device or a device requiring clinical trials.

    Therefore, I cannot fulfill your request for the information outlined in your prompt based on the provided text. The prompt asks for specific details about a study and acceptance criteria that are not present in this regulatory summary.

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