BEUDAMED
    FDA 510(k) FDA class 2 Substantially Equivalent 🇬🇧 United Kingdom

    MODIFICATION TO: YELLOPORT PORT ACCESS SYSTEM

    K Number: K070712 · Decision Mar 28, 2007
    View on FDA
    Classifications
    1
    FEI Numbers
    548
    Registration Numbers
    548
    Same Product Code
    1422
    Applicant Total
    2
    Review Days
    14

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    Basic Information

    Device Name
    MODIFICATION TO: YELLOPORT PORT ACCESS SYSTEM
    K Number
    K070712
    Device Class
    FDA class 2
    Clearance Type
    Special
    Regulation Number
    876.1500
    Medical Specialty
    Gastroenterology, Urology
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Surgical Innovations Group Plc
    Date Received
    March 14, 2007
    Decision Date
    March 28, 2007
    Product Code
    GCJ
    Advisory Committee
    Gastroenterology, Urology
    Review Advisory Committee
    SU
    Third Party
    Y

    Classifications

    This FDA 510(k) entry is associated with 1 FDA classification via its product code.

    Product Code Device Name
    GCJ Laparoscope, General & Plastic Surgery

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    Other Clearances by Surgical Innovations Group Plc

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