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

    MODEL CF-300 THREE CHANNEL FLOW METER

    K Number: K792190 · Decision Nov 21, 1979
    View on FDA
    Classifications
    1
    FEI Numbers
    36
    Registration Numbers
    36
    Same Product Code
    26
    Applicant Total
    2
    Review Days
    21

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    Basic Information

    Device Name
    MODEL CF-300 THREE CHANNEL FLOW METER
    K Number
    K792190
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    870.2060
    Medical Specialty
    Cardiovascular
    Decision
    Substantially Equivalent
    Applicant
    Wilton Webster Laboratories
    Date Received
    October 31, 1979
    Decision Date
    November 21, 1979
    Product Code
    DRQ
    Advisory Committee
    Cardiovascular
    Review Advisory Committee
    CV
    Third Party
    N

    Classifications

    This FDA 510(k) entry is associated with 1 FDA classification via its product code.

    Product Code Device Name
    DRQ Amplifier And Signal Conditioner, Transducer Signal

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    Other Clearances by Wilton Webster Laboratories

    K Number Device Name
    K780131 THERMOMETER, DIGITAL, NTM-100