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

    NEBULIZER/HUMIDIFIER HUMIDITY CENTER-MI.

    K Number: K810939 · Decision Apr 23, 1981
    View on FDA
    Classifications
    1
    FEI Numbers
    108
    Registration Numbers
    108
    Same Product Code
    220
    Applicant Total
    26
    Review Days
    16

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    Basic Information

    Device Name
    NEBULIZER/HUMIDIFIER HUMIDITY CENTER-MI.
    K Number
    K810939
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    868.5450
    Medical Specialty
    Anesthesiology
    Decision
    Substantially Equivalent
    Applicant
    Allied Healthcare Products, Inc.
    Date Received
    April 7, 1981
    Decision Date
    April 23, 1981
    Product Code
    BTT
    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
    BTT Humidifier, Respiratory Gas, (Direct Patient Interface)

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