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

    LEEP SYSTEM 6000 ELECTROSURGICAL UNIT AND ACCESSOR

    K Number: K905747 · Decision Sep 17, 1991
    View on FDA
    Classifications
    1
    FEI Numbers
    66
    Registration Numbers
    66
    Same Product Code
    52
    Applicant Total
    2
    Review Days
    267

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    Basic Information

    Device Name
    LEEP SYSTEM 6000 ELECTROSURGICAL UNIT AND ACCESSOR
    K Number
    K905747
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    884.4120
    Medical Specialty
    Obstetrics/Gynecology
    Decision
    Substantially Equivalent
    Applicant
    Coopervision Surgical
    Date Received
    December 24, 1990
    Decision Date
    September 17, 1991
    Product Code
    HGI
    Advisory Committee
    Obstetrics/Gynecology
    Review Advisory Committee
    OB
    Third Party
    N

    Classifications

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

    Product Code Device Name
    HGI Electrocautery, Gynecologic (And Accessories)

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    Other Clearances by Coopervision Surgical

    K Number Device Name
    K921390 XENON LIGHT SOURCE AND ACCESSORIES