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

    LAPAROSCAN(TM) INTRAOPER DIAG ULTRASOUND SYSTEM

    K Number: K913472 · Decision Mar 13, 1992
    View on FDA
    Classifications
    1
    FEI Numbers
    388
    Registration Numbers
    389
    Same Product Code
    407
    Applicant Total
    503
    Review Days
    221

    Basic Information

    Device Name
    LAPAROSCAN(TM) INTRAOPER DIAG ULTRASOUND SYSTEM
    K Number
    K913472
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    892.1570
    Medical Specialty
    Radiology
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    BAXTER HEALTHCARE CORP.
    Date Received
    August 5, 1991
    Decision Date
    March 13, 1992
    Product Code
    ITX
    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
    ITX Transducer, Ultrasonic, Diagnostic

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