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

    PATIENT MOVER(TM)

    K Number: K890555 · Decision Feb 13, 1989
    View on FDA
    Classifications
    1
    FEI Numbers
    5
    Registration Numbers
    5
    Same Product Code
    35
    Applicant Total
    2
    Review Days
    7

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    Basic Information

    Device Name
    PATIENT MOVER(TM)
    K Number
    K890555
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    890.5150
    Medical Specialty
    Physical Medicine
    Decision
    Substantially Equivalent
    Applicant
    T.B.S., Inc.
    Date Received
    February 6, 1989
    Decision Date
    February 13, 1989
    Product Code
    ILK
    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
    ILK Transport, Patient, Powered

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    Other Clearances by T.B.S., Inc.

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