BEUDAMED
    FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

    MISER INHALATION DEVICE, PART NO. 700

    K Number: K800763 · Decision Apr 24, 1980
    View on FDA
    Classifications
    1
    FEI Numbers
    140
    Registration Numbers
    140
    Same Product Code
    61
    Applicant Total
    1
    Review Days
    17

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    Basic Information

    Device Name
    MISER INHALATION DEVICE, PART NO. 700
    K Number
    K800763
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    868.5640
    Medical Specialty
    Anesthesiology
    Decision
    Substantially Equivalent
    Applicant
    Vix Breathing Equipment Co.
    Date Received
    April 7, 1980
    Decision Date
    April 24, 1980
    Product Code
    CCQ
    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
    CCQ Nebulizer, Medicinal, Non-Ventilatory (Atomizer)

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