BEUDAMED
    FDA PMA FDA Class 3 Approved 🇺🇸 United States

    Intraocular Lens

    PMA: P940007 · Supplement: S006 · Decision Apr 2, 2001
    View on FDA
    Classifications
    1
    FEI Numbers
    59
    Registration Numbers
    59

    Basic Information

    Device Name
    Intraocular Lens
    Trade Name
    CEEON SILICONE POSTERIOR CHAMBER INTRAOCULAR LENSES
    PMA Number
    P940007
    Supplement Number
    S006
    Device Class
    FDA Class 3
    Product Code
    HQL
    Generic Name
    intraocular lens
    Regulation Number
    886.3600
    Medical Specialty
    Ophthalmic
    Advisory Committee
    Ophthalmic
    Decision
    Approved
    Decision Code
    APPR
    Decision Date
    April 2, 2001
    Date Received
    September 5, 2000
    Supplement Type
    Normal 180 Day Track
    Supplement Reason
    Express GMP Supplement
    Expedited Review
    N

    Advisory Committee Statement

    APPROVAL FOR STERILIZING THE SILICONE POSTERIOR CHAMBER INTRAOCULAR LENS, MODEL 912, AT THE FACILITY IN GRONINGEN, THE NETHERLAND AND FOR CHANGES IN THE STERILIZATION CYCLE PARAMETERS FOR MODEL 912 FROM 100% ETHYLENE OXIDE (ET0) TO 20 % ET0/80% CARBON DIOXIDE.

    Classifications

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

    Product Code Device Name
    HQL Intraocular Lens