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

    SEQUOIA PLUS DIAGNOSTIC ULTRASOUND SYSTEM

    K Number: K072365 · Decision Oct 17, 2007
    View on FDA
    Classifications
    1
    FEI Numbers
    220
    Registration Numbers
    220
    Same Product Code
    1171
    Applicant Total
    11
    Review Days
    55

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    Basic Information

    Device Name
    SEQUOIA PLUS DIAGNOSTIC ULTRASOUND SYSTEM
    K Number
    K072365
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    892.1550
    Medical Specialty
    Radiology
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Siemens Medical Solutions USA, Inc., Ultrasound DI
    Date Received
    August 23, 2007
    Decision Date
    October 17, 2007
    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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