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

    VERSAPOINT RESECTOSCOPIC SYSTEM

    K Number: K040302 · Decision Mar 9, 2004
    View on FDA
    Classifications
    1
    FEI Numbers
    135
    Registration Numbers
    135
    Same Product Code
    170
    Applicant Total
    2
    Review Days
    29

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    Basic Information

    Device Name
    VERSAPOINT RESECTOSCOPIC SYSTEM
    K Number
    K040302
    Device Class
    FDA class 2
    Clearance Type
    Special
    Regulation Number
    884.1690
    Medical Specialty
    Obstetrics/Gynecology
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Gynecare, A Div. of Ethicon, Inc.
    Date Received
    February 9, 2004
    Decision Date
    March 9, 2004
    Product Code
    HIH
    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
    HIH Hysteroscope (And Accessories)

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    Other Clearances by Gynecare, A Div. of Ethicon, Inc.

    K Number Device Name
    K013718 GYNEMESH PROLENE SOFT (POLYPROPYLENE) NONABSORBABLE SYNTHETIC SURGICAL MESH FOR PELVIC FLOOR REPAIR