BEUDAMED
    FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

    LIFTKAR PT

    K Number: K110495 · Decision May 20, 2011
    View on FDA
    Classifications
    1
    FEI Numbers
    5
    Registration Numbers
    5
    Same Product Code
    28
    Applicant Total
    1
    Review Days
    87

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    Basic Information

    Device Name
    LIFTKAR PT
    K Number
    K110495
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    890.3930
    Medical Specialty
    Physical Medicine
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Sano Transportgerate GmbH
    Date Received
    February 22, 2011
    Decision Date
    May 20, 2011
    Product Code
    ING
    Advisory Committee
    Physical Medicine
    Review Advisory Committee
    PM
    Third Party
    N

    Classifications

    This FDA 510(k) entry is associated with 1 FDA classification via its product code.

    Product Code Device Name
    ING Elevator, Wheelchair, Portable

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