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

    SSD-650 LINEAR, CONVEX SECTOR, ULTRASOUND SCANNING

    K Number: K871400 · Decision Jul 24, 1987
    View on FDA
    Classifications
    1
    FEI Numbers
    6
    Registration Numbers
    6
    Same Product Code
    77
    Applicant Total
    136
    Review Days
    107

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    Basic Information

    Device Name
    SSD-650 LINEAR, CONVEX SECTOR, ULTRASOUND SCANNING
    K Number
    K871400
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    870.2330
    Medical Specialty
    Cardiovascular
    Decision
    Substantially Equivalent
    Applicant
    Ge Medical Systems Information Technologies
    Date Received
    April 8, 1987
    Decision Date
    July 24, 1987
    Product Code
    DXK
    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
    DXK Echocardiograph

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