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

    CONTINUOUS WAVE DOPPLER

    K Number: K760751 · Decision Oct 13, 1976
    View on FDA
    Classifications
    1
    FEI Numbers
    44
    Registration Numbers
    44
    Same Product Code
    136
    Applicant Total
    4
    Review Days
    12

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    Basic Information

    Device Name
    CONTINUOUS WAVE DOPPLER
    K Number
    K760751
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    870.2100
    Medical Specialty
    Cardiovascular
    Decision
    Substantially Equivalent
    Applicant
    Medsonics
    Date Received
    October 1, 1976
    Decision Date
    October 13, 1976
    Product Code
    DPW
    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
    DPW Flowmeter, Blood, Cardiovascular

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    Other Clearances by Medsonics

    K Number Device Name
    K770904 PROBE, BLOOD FLOW DETECTOR PLUG-IN
    K770332 AMPLIFIER, PHOTOPULSE, MODEL PA13
    K760728 CONTINUOUS WAVE DOPPLER ULTRASOUND