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

    VERSAPORT V2 BLADELESS OPTICAL TROCAR

    K Number: K130435 · Decision Mar 14, 2013
    View on FDA
    Classifications
    1
    FEI Numbers
    573
    Registration Numbers
    573
    Same Product Code
    1391
    Applicant Total
    13
    Review Days
    21

    Basic Information

    Device Name
    VERSAPORT V2 BLADELESS OPTICAL TROCAR
    K Number
    K130435
    Device Class
    FDA class 2
    Clearance Type
    Special
    Regulation Number
    876.1500
    Medical Specialty
    Gastroenterology, Urology
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    COVIDIEN, FORMERLY US SURGICAL A DIVISON OF TYCO H
    Date Received
    February 21, 2013
    Decision Date
    March 14, 2013
    Product Code
    GCJ
    Advisory Committee
    Gastroenterology, Urology
    Review Advisory Committee
    SU
    Third Party
    N

    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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