BEUDAMED
    FDA 510(k) FDA class 2 Unknown 🇨🇦 Canada

    QUICKAIR CHOKE RELIEVER, MODEL 59-001A

    K Number: DEN000004 · Decision Feb 29, 2000
    View on FDA
    Classifications
    1
    FEI Numbers
    2
    Registration Numbers
    2
    Same Product Code
    0
    Applicant Total
    1
    Review Days
    32

    Basic Information

    Device Name
    QUICKAIR CHOKE RELIEVER, MODEL 59-001A
    K Number
    DEN000004
    Device Class
    FDA class 2
    Clearance Type
    Post-NSE
    Regulation Number
    868.5115
    Medical Specialty
    Anesthesiology
    Decision
    Unknown
    Applicant
    MAET INDUSTRIES, INC.
    Date Received
    January 28, 2000
    Decision Date
    February 29, 2000
    Product Code
    MZT
    Advisory Committee
    Anesthesiology
    Review Advisory Committee
    AN
    Third Party
    N

    Classifications

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

    Product Code Device Name
    MZT Device, Heimlich Maneuver Assist