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

    VMT HAND HELD NEBULIZER

    K Number: K841894 · Decision Jun 5, 1984
    View on FDA
    Classifications
    1
    FEI Numbers
    140
    Registration Numbers
    140
    Same Product Code
    61
    Applicant Total
    28
    Review Days
    29

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    Basic Information

    Device Name
    VMT HAND HELD NEBULIZER
    K Number
    K841894
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    868.5640
    Medical Specialty
    Anesthesiology
    Decision
    Substantially Equivalent
    Applicant
    Vortran Medical Technology 1, Inc.
    Date Received
    May 7, 1984
    Decision Date
    June 5, 1984
    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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