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510(k) Data Aggregation

    K Number
    K171261
    Manufacturer
    Date Cleared
    2017-08-18

    (109 days)

    Product Code
    Regulation Number
    892.1750
    Reference & Predicate Devices
    N/A
    Predicate For
    N/A
    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
    Intended Use

    Scannerside Dose check is intended for providing Computed Tomographic (CT) Dose Check feature to CT X-ray systems. The Scannerside Dose Check is specifically indicated for providing the Computed Tomography Dose Check feature with notifies and alerts the CT equipment operators, prior to a scan, if the estimated dose is above a predefined threshold. This device is intended for CT scanners not equipped with this functionality. The device is indicated for use by professional personnel.

    Device Description

    Not Found

    AI/ML Overview

    This document is an FDA 510(k) clearance letter for a device called "ScannerSide DoseCheck." It doesn't contain information about the device's technical specifications, acceptance criteria, or the study conducted to prove it meets those criteria. The letter primarily states that the device has been determined to be substantially equivalent to legally marketed predicate devices.

    Therefore, I cannot provide the requested information based on the provided text. The document does not describe acceptance criteria, nor does it detail a study proving device performance against such criteria. It's a regulatory clearance, not a technical performance report.

    To answer your request, I would need a document from Right Dose Inc. (the manufacturer) that details their V&V (Verification and Validation) study for the ScannerSide DoseCheck device, including the testing methodology, acceptance criteria, and study results.

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