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

    ACUSON S2000 DIAGNOSTIC ULTRASOUND SYSTEM

    K Number: K090334 · Decision Feb 20, 2009
    View on FDA
    Classifications
    1
    FEI Numbers
    220
    Registration Numbers
    220
    Same Product Code
    1171
    Applicant Total
    32
    Review Days
    10

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    Basic Information

    Device Name
    ACUSON S2000 DIAGNOSTIC ULTRASOUND SYSTEM
    K Number
    K090334
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    892.1550
    Medical Specialty
    Radiology
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Siemens Medi Cal Solutions, Inc.
    Date Received
    February 10, 2009
    Decision Date
    February 20, 2009
    Product Code
    IYN
    Advisory Committee
    Radiology
    Review Advisory Committee
    RA
    Third Party
    Y

    Classifications

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

    Product Code Device Name
    IYN System, Imaging, Pulsed Doppler, Ultrasonic

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