BEUDAMED
    FDA PMA FDA Class 3 Approved 🇺🇸 United States

    Laparoscopic Contraceptive Tubal Occlusion Device

    PMA: P070022 · Supplement: S019 · Decision May 27, 2011
    View on FDA
    Classifications
    1
    FEI Numbers
    7
    Registration Numbers
    7

    Basic Information

    Device Name
    Laparoscopic Contraceptive Tubal Occlusion Device
    Trade Name
    ADIANA PERMANENT CONTRACEPTION SYSTEM
    PMA Number
    P070022
    Supplement Number
    S019
    Device Class
    FDA Class 3
    Product Code
    KNH
    Generic Name
    Laparoscopic contraceptive tubal occlusion device
    Regulation Number
    884.5380
    Medical Specialty
    Obstetrics/Gynecology
    Advisory Committee
    Obstetrics/Gynecology
    Decision
    Approved
    Decision Code
    APPR
    Decision Date
    May 27, 2011
    Date Received
    April 13, 2011
    Supplement Type
    Normal 180 Day Track No User Fee
    Supplement Reason
    Location Change - Manufacturer/Sterilizer/Packager/Supplier
    Expedited Review
    N

    Advisory Committee Statement

    APPROVAL OF A BACKUP STERILIZATION FACILITY LOCATED AT BIOTEST LABORATORIES, INC., IN BROOKLYN PARK, MINNESOTA.

    Classifications

    This FDA Pre-Market Approval entry is associated with 1 FDA classification via its product code.

    Product Code Device Name
    KNH Laparoscopic Contraceptive Tubal Occlusion Device