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510(k) Data Aggregation

    K Number
    K041054
    Device Name
    MEDLINE STRIDER MAXI 3
    Manufacturer
    MEDLINE INDUSTRIES, INC.
    Date Cleared
    2004-05-25

    (32 days)

    Product Code
    INI
    Regulation Number
    890.3800
    Type
    Traditional
    Panel
    Physical Medicine
    Reference & Predicate Devices
    N/A
    Predicate For
    N/A
    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
    Intended Use

    The intended use of the Medline Strider MAXI 3 scooter is to provide mobility to persons that have difficulty walking for prolonged periods of time. They are intended to increase the mobility of persons who are both physically and mentally capable of assessing and reacting to any driving situation.

    The Medline Strider MAXI 3 scooter is constructed for use both indoors and outdoors. They are for use indoors, on pavement, sidewalks, pedestrian zones and arcas free from motor traffic. They must not be driven on public roads with the exception of crossing or when no pavements are available.

    Device Description

    Not Found

    AI/ML Overview

    The provided document is a 510(k) premarket notification letter from the FDA for a motorized three-wheeled vehicle (scooter). It does not contain information about the acceptance criteria, study details, or performance of a device in the context of an AI/medical imaging study.

    Therefore, I cannot extract the requested information about acceptance criteria, study design, expert ground truth, or AI performance. The document pertains to the regulatory clearance of a physical medical device (a scooter), not a diagnostic algorithm or image analysis software.

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