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510(k) Data Aggregation

    K Number
    K052344
    Date Cleared
    2005-09-14

    (19 days)

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

    COLOR LCD MONITOR, MODEL RADIOFORCE R31 & R31-C

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

    RadiForce R31 and R31-C are intended to be used in displaying and viewing digital images for diagnosis of X-ray or MRI, etc. by trained medical practitioners. These devices must not be used for digital mammography system.

    Device Description

    RadiForce R31 and R31-C are 53cm (20.8") Color LCD displays for medical viewing. Each model produces hi·crisp images for modality applications and 3D image fusion. The model difference between R31 and R31-C are the panel protector provided with R31-C and brightness only.

    AI/ML Overview

    This 510(k) premarket notification (K052344) is for a medical display device, the EIZO NANAO CORPORATION’s Color LCD Monitor, RadiForce R31 and R31-C. It does not contain information about an AI/ML device or its performance study. Therefore, I cannot accurately answer your request.

    Medical displays like the RadiForce R31 are evaluated based on display hardware performance specifications (e.g., luminance, resolution, contrast ratio, uniformity, color accuracy) and their ability to render medical images accurately, not on clinical performance metrics like diagnostic accuracy, sensitivity, or specificity that would be generated from a study involving image interpretation by human readers or an AI algorithm.

    The provided documentation does not include:

    • Acceptance criteria and reported device performance in terms of clinical outcomes or diagnostic accuracy.
    • Sample sizes for test sets, data provenance, or ground truth establishment.
    • Details about expert involvement, adjudication methods, or MRMC studies.
    • Standalone algorithm performance or training set information.

    Instead, the documentation focuses on the substantial equivalence of the new device to a predicate device (RadiForce R22) based on technical characteristics and intended use for displaying digital images for diagnosis.

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