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

    GE LOGIQ BT08 DIAGNOSTIC ULTRASOUND SYSTEM

    K Number: K073408 · Decision Dec 19, 2007
    View on FDA
    Classifications
    1
    FEI Numbers
    220
    Registration Numbers
    220
    Same Product Code
    1171
    Applicant Total
    7
    Review Days
    15

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    Basic Information

    Device Name
    GE LOGIQ BT08 DIAGNOSTIC ULTRASOUND SYSTEM
    K Number
    K073408
    Device Class
    FDA class 2
    Clearance Type
    Special
    Regulation Number
    892.1550
    Medical Specialty
    Radiology
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Ge Medical Systems Ultrasound and Primary Care Dia
    Date Received
    December 4, 2007
    Decision Date
    December 19, 2007
    Product Code
    IYN
    Advisory Committee
    Radiology
    Review Advisory Committee
    RA
    Third Party
    N

    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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    Other Clearances by Ge Medical Systems Ultrasound and Primary Care Dia

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    K072439 GE LUNAR DPX & PRODIGY SERIES DEXA BONE DENSITOMETERS WITH MOBILE KIT
    K052581 LUNAR IDXA
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