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

    CINEMEASURE (TM)

    K Number: K910654 · Decision Jun 6, 1991
    View on FDA
    Classifications
    1
    FEI Numbers
    123
    Registration Numbers
    123
    Same Product Code
    198
    Applicant Total
    1
    Review Days
    112

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    Basic Information

    Device Name
    CINEMEASURE (TM)
    K Number
    K910654
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    892.1600
    Medical Specialty
    Radiology
    Decision
    Substantially Equivalent
    Applicant
    Syracuse Research Corp.
    Date Received
    February 14, 1991
    Decision Date
    June 6, 1991
    Product Code
    IZI
    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
    IZI System, X-Ray, Angiographic

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