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510(k) Data Aggregation

    K Number
    K191188
    Device Name
    ASHK100G
    Manufacturer
    Date Cleared
    2019-05-30

    (27 days)

    Product Code
    Regulation Number
    892.2050
    Reference & Predicate Devices
    Predicate For
    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
    Intended Use

    Software used in a device that saves, enlarges, reduces, views as well as analyzes, transfers and prints medical images. (excluding fluoroscopic, angiographic, and mammographic applications.)

    Device Description

    ASHK100G is digital radiography operating console software. ASHK100G provides an integrated solution for X-ray projection. It integrates with the digital detector. Furthermore, ASHK100G acquires and processes images. In addition, it complies with DICOM standards and is able to transmit and receive data with the PACS system, and print images through the DICOM printer.

    AI/ML Overview

    This document, a 510(k) premarket notification for the ASHK100G device, indicates that clinical testing was not applicable for this submission. Therefore, it does not contain the information required to answer the questions about acceptance criteria, device performance, sample sizes, ground truth establishment, or clinical study methodologies.

    The document primarily focuses on demonstrating substantial equivalence to a predicate device (Rayence Co., Ltd.'s XmaruView V1, Xmaru Chiroview, Xmaru Podview, and Xmaru PACS) based on technological characteristics and indications for use, rather than clinical performance data.

    Specifically, page 8, section 9, explicitly states: "Clinical Test Summary [21 CFR 807.92(b)(2)] This section is not applicable."

    As a result, I cannot provide the requested details about acceptance criteria and study findings.

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