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510(k) Data Aggregation

    K Number
    K143157
    Manufacturer
    Date Cleared
    2014-11-12

    (9 days)

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

    The Coronis Fusion 4MP LED (MDCC-4230) Medical Flat Panel Display System is intended to be used as a tool in displaying and viewing digital images (excluding digital mammography) for review and analysis by trained medical practitioners.

    Device Description

    The Coronis Fusion 4MP LED (MDCC-4230) is a high-resolution flat panel LCD display system for reviewing medical images. It consists of an LCD display (MDCC-4230), an optional high-resolution display controller board and QA software. The display controller board is installed in a PACS workstation computer, connected to the display. The QA software helps to make and keep the displays DICOM compliant. The display uses LED backlight technology.

    AI/ML Overview

    The provided document is a 510(k) summary for the Barco Coronis Fusion 4MP LED (MDCC-4230) Medical Flat Panel Display System, which is a display device, not an AI/ML medical device. Therefore, the information typically requested for AI/ML device studies (such as sample size for test/training sets, ground truth methodology, expert qualifications, adjudication methods, MRMC studies, or standalone performance) is not applicable or provided within this document.

    The document focuses on demonstrating substantial equivalence to a predicate device (Coronis Fusion 4MP DL, MDCC-4130) by comparing technological characteristics and presenting bench test results related to safety and performance.

    Here's a breakdown of the available information relevant to acceptance criteria and device performance:

    1. Table of Acceptance Criteria (implicitly, comparison to predicate) and Reported Device Performance:

    The document doesn't explicitly state "acceptance criteria" as pass/fail thresholds for clinical performance but rather demonstrates equivalence to a predicate device based on similar or superior characteristics as shown in a table comparing specifications and the results of bench testing.

    CharacteristicPredicate Device (MDCC-4130) ValueSubject Device (MDCC-4230) ValuePerformance Description / Test Result
    General
    Screen technologyTFT AM LCD Dual Domain IPS ProTFT AM LCD Dual Domain IPS ProSame
    Active screen size (diagonal)756 mm (29.8")756 mm (29.8")Same
    Active screen size (H x V)641.28 x 400.8 mm (25.2 x 15.8")641.28 x 400.8 mm (25.2 x 15.8")Same
    Aspect ratio (H:V)16:1016:10Same
    Resolution4MP (2560 x 1600)4MP (2560 x 1600)Same
    Pixel pitch0.2505 mm0.2505 mmSame
    Color imagingYesYesSame
    Gray imagingNoNoSame
    Viewing angle (H, V)178°178°Same
    Uniform Luminance Technology (ULT)YesYesSame
    Ambient Light Compensation (ALC)YesYesSame
    Backlight Output Stabilization (BLOS)YesYesSame
    I-GuardYesYesSame
    DICOM calibrated luminance (ULT off)500 cd/m²500 cd/m²Same
    Response time (Tr + Tf)20 ms20 msSame
    Scanning frequency (H; V)30-150 kHz; 15-80 Hz30-150 kHz; 15-80 HzSame
    Video input signalsDVI-D Dual LinkDVI-D Dual Link / DisplayPort 1.1Improvement: Added DisplayPort 1.1
    USB ports1 upstream (endpoint), 3 downstream (USB 1.0)1 upstream (endpoint), 3 downstream (USB 2.0)Improvement: Upgraded to USB 2.0
    Power requirements (nominal)100-240V100-240VSame
    Power save modeYesYesSame
    Differences/Improvements
    Backlight technologyCCFLLEDImprovement: LED backlight instead of CCFL. Tested via DICOM calibration and Luminance Uniformity tests.
    Per Pixel Uniformity (PPU)No (per zone uniformity)YesImprovement: Per Pixel Uniformity. Tested via Luminance Uniformity tests.
    Maximum luminance950 cd/m²720 cd/m²Different, but considered acceptable within the context of medical imaging display standards and DICOM calibration targets.
    Contrast ratio (typical)1100:11000:1Different, but considered acceptable.
    Power consumption (nominal)135W105WImprovement: Lower power consumption.
    Net weight with stand28.1 kg21.5 kgImprovement: Lighter.
    Net weight w/o stand21.6 kg15 kgImprovement: Lighter.
    FirmwareSpecific to MDCC-4130New (different platform)Firmware tests performed.
    Front filter materialUnspecifiedDifferent materialImpact test in IEC 60601-1 tests.
    Sheet metal parts materialUnspecifiedOther materialShock and Vibration tests in Environmental test report.
    Electrical SafetyConformed to standardsConforms to IEC 60601-1Additional test performed: Electrical Safety test (IEC 60601-1).
    EMCConformed to standardsConforms to IEC 60601-1-2Additional test performed: EMC test (IEC 60601-1-2).

    The conclusion states: "The tests showed that the device has similar or superior characteristics compared to the predicate device and did not reveal new issues of safety and performance."


    The questions about sample size, ground truth, experts, adjudication, and MRMC studies are not applicable to this type of device (a medical display monitor) and therefore are not found in the provided document. The device is evaluated based on its physical and technical specifications, and its ability to meet relevant performance and safety standards, rather than its interpretive output on medical images. No animal or clinical testing was performed.

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