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

    FORTRESS COMMUTER RT (RIGID TRANSPORT)

    K Number: K901708 · Decision Apr 20, 1990
    View on FDA
    Classifications
    1
    FEI Numbers
    121
    Registration Numbers
    121
    Same Product Code
    550
    Applicant Total
    2
    Review Days
    7

    Basic Information

    Device Name
    FORTRESS COMMUTER RT (RIGID TRANSPORT)
    K Number
    K901708
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    890.3860
    Medical Specialty
    Physical Medicine
    Decision
    Substantially Equivalent
    Applicant
    FORTRESS, INC.
    Date Received
    April 13, 1990
    Decision Date
    April 20, 1990
    Product Code
    ITI
    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
    ITI Wheelchair, Powered

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    Other Clearances by FORTRESS, INC.

    K Number Device Name
    K901707 FORTRESS COMMUTER FT (FOLDING TRANSPORT)