BEUDAMED
    FDA 510(k) FDA class 2 Substantially Equivalent 🇮🇪 Ireland

    AERONEB PROFESSIONAL NEBULIZER SYSTEM

    K Number: K070642 · Decision May 7, 2007
    View on FDA
    Classifications
    1
    FEI Numbers
    189
    Registration Numbers
    189
    Same Product Code
    507
    Applicant Total
    2
    Review Days
    60

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    Basic Information

    Device Name
    AERONEB PROFESSIONAL NEBULIZER SYSTEM
    K Number
    K070642
    Device Class
    FDA class 2
    Clearance Type
    Special
    Regulation Number
    868.5630
    Medical Specialty
    Anesthesiology
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    Aerogen (Ireland), Ltd.
    Date Received
    March 8, 2007
    Decision Date
    May 7, 2007
    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 Aerogen (Ireland), Ltd.

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