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510(k) Data Aggregation

    K Number
    K983526
    Device Name
    VERTICAL LIFT
    Manufacturer
    BARNES,RICHARDSON & COLBURN
    Date Cleared
    1998-12-11

    (64 days)

    Product Code
    ING
    Regulation Number
    890.3930
    Type
    Traditional
    Panel
    Physical Medicine
    Reference & Predicate Devices
    N/A
    Why did this record match?
    Device Name :

    VERTICAL LIFT

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

    The Vertical Lift is intended to mechanically transport one person in a wheelchair or in a standing position over stairs in a private or public facility either indoors or outdoors.

    Device Description

    Vertical Platform Lift

    AI/ML Overview

    This is a notification of intent to market a device, it is not a study. As such, the input does not contain information about acceptance criteria or a study that proves the device meets acceptance criteria. The document is a 510(k) clearance letter for a "Vertical Lift" device, indicating that the FDA has found it substantially equivalent to previously marketed devices.

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