BEUDAMED
    FDA PMA FDA Class 2 Approved (Reclassification) 🇺🇸 United States

    Changer, Tube, Endotracheal

    PMA: P800068 · Decision Jul 21, 1981
    View on FDA
    Classifications
    1
    FEI Numbers
    2
    Registration Numbers
    2

    Basic Information

    Device Name
    Changer, Tube, Endotracheal
    Trade Name
    ENDOTRACHEAL TUBE CHANGER
    PMA Number
    P800068
    Device Class
    FDA Class 2
    Product Code
    LNZ
    Generic Name
    Changer, tube, endotracheal
    Regulation Number
    868.5730
    Medical Specialty
    Anesthesiology
    Advisory Committee
    Anesthesiology
    Decision
    Approved (Reclassification)
    Decision Code
    APRL
    Decision Date
    July 21, 1981
    Date Received
    November 21, 1980
    Expedited Review
    N

    Classifications

    This FDA Pre-Market Approval entry is associated with 1 FDA classification via its product code.

    Product Code Device Name
    LNZ Changer, Tube, Endotracheal