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

    VS, ANESTHESIA VENTILATOR

    K Number: K790809 · Decision May 4, 1979
    View on FDA
    Classifications
    1
    FEI Numbers
    130
    Registration Numbers
    130
    Same Product Code
    504
    Applicant Total
    13
    Review Days
    8

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    Basic Information

    Device Name
    VS, ANESTHESIA VENTILATOR
    K Number
    K790809
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    868.5895
    Medical Specialty
    Anesthesiology
    Decision
    Substantially Equivalent
    Applicant
    Airco/Ohio Medical Products
    Date Received
    April 26, 1979
    Decision Date
    May 4, 1979
    Product Code
    CBK
    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
    CBK Ventilator, Continuous, Facility Use

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    Other Clearances by Airco/Ohio Medical Products

    K Number Device Name
    K833459 COAXIAL VOL. VENTILATOR CIRCUIT
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    K832185 OHIO MODEL 922 SPIROMETER
    K830446 OXYGEN MONITOR OHIO 5100
    K822456 OHIO V5A ANESTHESIA VENTILATOR
    K813476 OHIO VOLUME INCENTIVE SPIROMETER
    K812879 OHIO NON-REUSABLE TRACHEAL TUBE MURPHY
    K812880 OHIO NON-REUSABLE TRACHEAL TUBE MAJILL
    Search all 13 clearances from Airco/Ohio Medical Products →