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

    ASTHMAKIT

    K Number: K874047 · Decision Feb 29, 1988
    View on FDA
    Classifications
    1
    FEI Numbers
    189
    Registration Numbers
    189
    Same Product Code
    507
    Applicant Total
    43
    Review Days
    147

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    Basic Information

    Device Name
    ASTHMAKIT
    K Number
    K874047
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    868.5630
    Medical Specialty
    Anesthesiology
    Decision
    Substantially Equivalent
    Applicant
    Dhd Medical Products Div. Diemolding Corp.
    Date Received
    October 5, 1987
    Decision Date
    February 29, 1988
    Product Code
    CAF
    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
    CAF Nebulizer (Direct Patient Interface)

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    Other Clearances by Dhd Medical Products Div. Diemolding Corp.

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    K860873 VENTURI MASK/ADULT & PAEDIATRIC
    K860879 DISPOSABLE VENTILATOR CIRCUITS
    K860880 VENTILATOR CIRCUITS (VARIOUS TYPES)
    K860878 BRITISH BREATHING CIRCUIT SYSTEM
    K860877 FLEXTUBE, CONNECTING TUBING
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