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

    ARTHROCARE UROLOGY ELECTROSURGERY SYSTEM

    K Number: K010568 · Decision Mar 27, 2001
    View on FDA
    Classifications
    1
    FEI Numbers
    117
    Registration Numbers
    117
    Same Product Code
    187
    Applicant Total
    112
    Review Days
    29

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    Basic Information

    Device Name
    ARTHROCARE UROLOGY ELECTROSURGERY SYSTEM
    K Number
    K010568
    Device Class
    FDA class 2
    Clearance Type
    Special
    Regulation Number
    876.4300
    Medical Specialty
    Gastroenterology, Urology
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Arthrocare Corp.
    Date Received
    February 26, 2001
    Decision Date
    March 27, 2001
    Product Code
    KNS
    Advisory Committee
    Gastroenterology, Urology
    Review Advisory Committee
    GU
    Third Party
    N

    Classifications

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

    Product Code Device Name
    KNS Unit, Electrosurgical, Endoscopic (With Or Without Accessories)

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