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510(k) Data Aggregation

    K Number
    K061447
    Date Cleared
    2006-07-21

    (57 days)

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

    5M MONOCHROME DIGITAL MAMMOGRAPHY LCD MONITOR MDL2116A (ME551I2)

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

    5M Monochrome Digital Mammography LCD Monitor MDL2116A (ME551i2) 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

    MDL2116A (ME551i2) is a 21.3-inch 5 megapixel monochrome LCD monitor whose display resolution is 2048 x 2560 (QSXGA), supporting DVI (digital visual interface).

    AI/ML Overview

    The provided text is related to a 510(k) submission for a medical device, specifically a "5M Monochrome Digital Mammography LCD Monitor MDL2116A (ME551i2)". This document, however, does not contain a detailed study design or acceptance criteria for a device that uses an algorithm or AI. Instead, it's a regulatory submission for a display monitor that practitioners use to view medical images, including those from digital mammography.

    Therefore, many of the requested items, such as sample sizes for test/training sets, number of experts for ground truth, adjudication methods, MRMC studies, standalone algorithm performance, and types of ground truth, are not applicable to this type of device. These are typically relevant for AI/ML-driven diagnostic devices or advanced image processing software that generate a clinical output, not for a display monitor.

    The document primarily focuses on establishing substantial equivalence to a predicate device (ME511L (K0417337)) based on its technical specifications and intended use.

    Here's an attempt to address the relevant points based on the provided text, and explicitly state where information is not available or not applicable:

    1. A table of acceptance criteria and the reported device performance

    The document does not explicitly state acceptance criteria or performance metrics in a table format as would be expected for a diagnostic algorithm. The "reported device performance" for a monitor like this would typically involve technical specifications related to display quality, resolution, luminance, uniformity, and adherence to display standards for medical imaging (e.g., DICOM Part 14). While these are not detailed here, the statement of "Substantial Equivalence" implies that these performance aspects are at least comparable to the predicate device.

    Acceptance Criteria (Implied / Not Explicitly Stated for this Device Type)Reported Device Performance (Implied from Substantial Equivalence and Device Description)
    Display Resolution2048 x 2560 (QSXGA)
    Display Type21.3-inch 5 megapixel monochrome LCD monitor
    ConnectivitySupporting DVI (digital visual interface)
    Intended UseDisplaying/viewing medical images for diagnosis, including digital mammography PACS and FFDM.
    Substantial Equivalence to PredicateSame characteristics as ME511L (K041737) except for board, power supply, and front sensor.

    2. Sample size used for the test set and the data provenance

    Not Applicable. This is a hardware display monitor. There is no "test set" of medical images in the context of evaluating an algorithm's performance. The evaluation would involve technical testing of the monitor's display characteristics, not an analysis of a dataset of medical images.

    3. Number of experts used to establish the ground truth for the test set and the qualifications of those experts

    Not Applicable. As above, there is no "ground truth" establishment for a test set of medical images in the context of this device. The assessment is technical verification of monitor specifications and image display capabilities.

    4. Adjudication method for the test set

    Not Applicable. No test set of medical images requiring adjudication.

    5. If a multi-reader multi-case (MRMC) comparative effectiveness study was done, If so, what was the effect size of how much human readers improve with AI vs without AI assistance

    Not Applicable. This is a display monitor, not an AI or algorithm-driven diagnostic device. MRMC studies are used to evaluate the impact of a new diagnostic method (often involving AI) on human reader performance.

    6. If a standalone (i.e. algorithm only, without human-in-the-loop performance) was done

    Not Applicable. This device is a display monitor and does not involve an algorithm or AI that operates in a standalone capacity.

    7. The type of ground truth used (expert consensus, pathology, outcomes data, etc)

    Not Applicable. No ground truth needed for a clinical study comparing an algorithm's performance. The "truth" for a monitor is its technical specifications meeting established display standards.

    8. The sample size for the training set

    Not Applicable. This is a hardware monitor; there is no "training set" in the context of machine learning.

    9. How the ground truth for the training set was established

    Not Applicable. No training set exists for this device.

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