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

    MODEL 54 FLOWMETER BACK-PRESSURE TUBE

    K Number: K791648 · Decision Sep 17, 1979
    View on FDA
    Classifications
    1
    FEI Numbers
    44
    Registration Numbers
    44
    Same Product Code
    23
    Applicant Total
    2
    Review Days
    24

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    Basic Information

    Device Name
    MODEL 54 FLOWMETER BACK-PRESSURE TUBE
    K Number
    K791648
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    868.2340
    Medical Specialty
    Anesthesiology
    Decision
    Substantially Equivalent
    Applicant
    Harris Calorific
    Date Received
    August 24, 1979
    Decision Date
    September 17, 1979
    Product Code
    CAX
    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
    CAX Flowmeter, Tube, Thorpe, Back-Pressure Compensated

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