BEUDAMED
    FDA 510(k) FDA class 2 Substantially Equivalent 🇮🇱 Israel

    THE IC-PRO SYSTEM

    K Number: K110256 · Decision May 27, 2011
    View on FDA
    Classifications
    1
    FEI Numbers
    155
    Registration Numbers
    155
    Same Product Code
    195
    Applicant Total
    8
    Review Days
    119

    Basic Information

    Device Name
    THE IC-PRO SYSTEM
    K Number
    K110256
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    892.1600
    Medical Specialty
    Radiology
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    PAIEON, INC.
    Date Received
    January 28, 2011
    Decision Date
    May 27, 2011
    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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