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    FDA 510(k) FDA class 2 Substantially Equivalent 🇹🇼 Taiwan

    ULTRASONIC NEBULIZER SYSTEM, MODEL KN-9210

    K Number: K083256 · Decision Jun 26, 2009
    View on FDA
    Classifications
    1
    FEI Numbers
    189
    Registration Numbers
    189
    Same Product Code
    507
    Applicant Total
    26
    Review Days
    234

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    Basic Information

    Device Name
    ULTRASONIC NEBULIZER SYSTEM, MODEL KN-9210
    K Number
    K083256
    Device Class
    FDA class 2
    Clearance Type
    Abbreviated
    Regulation Number
    868.5630
    Medical Specialty
    Anesthesiology
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    K-Jump Health Co., Ltd.
    Date Received
    November 4, 2008
    Decision Date
    June 26, 2009
    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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