Search Filters

Search Results

Found 1 results

510(k) Data Aggregation

    K Number
    K081242
    Date Cleared
    2008-06-11

    (41 days)

    Product Code
    Regulation Number
    892.2050
    Reference & Predicate Devices
    Why did this record match?
    Device Name :

    21.3 INCH (53CM) MONOCHROME DIGITAL MAMMOGRAPHY LCD MONITOR MS51I2, (MDL2123A)

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

    21.3 inch (53cm) Monochrome Digital Mammography 5M pixel LCD Monitor with subpixel driving techniques enabling 15M subpixels to be driven independently. MS51i2 (MDL2123A) is intended to be used in displaying and viewing medical images for diagnosis by trained medical practitioners. It is to be used in digital mammography PACS and modalities including FFDM.

    Device Description

    MS51i2 (MDL2123A) is a 21.3-inch (53 cm) monochrome LCD monitor whose display resolution is 2048 x 7680 (landscape), 7680 x 2048 (portrait) supporting DVI (digital visual interface).

    AI/ML Overview

    The provided text is a 510(k) summary for a medical display monitor (TOTOKU ELECTRIC CO., LTD. MS51i2). It describes the device, its intended use, and substantial equivalence to a predicate device. However, it does not contain information about acceptance criteria or a study proving the device meets performance criteria in the way that would be expected for an AI/CADe device.

    This document is a regulatory submission for a display monitor, which is a hardware component. Its performance is assessed differently than a software algorithm that performs analysis or detection. The key aspects of this submission revolve around demonstrating that the new monitor is substantially equivalent to an existing, legally marketed monitor, primarily focusing on hardware specifications and intended use.

    Therefore, I cannot fulfill the request to provide a table of acceptance criteria and reported device performance from this document, nor can I provide information on various study design elements (sample size, experts, adjudication, MRMC, standalone performance, ground truth, training set specifics) because these types of studies are not typically conducted or described for a display monitor's 510(k) submission.

    The 510(k) process for this device focuses on demonstrating that the monitor performs as expected for displaying medical images, not on its ability to interpret or detect findings. The acceptance criteria for such a device would likely pertain to display characteristics (resolution, brightness, contrast, color accuracy, uniformity), and testing would involve measurements against established standards (e.g., DICOM Part 14 calibration). This document does not detail those specific acceptance criteria or performance test results.

    Ask a Question

    Ask a specific question about this device

    Page 1 of 1