BEUDAMED
    FDA PMA FDA Class 3 Approved 🇺🇸 United States

    Aid, Surgical, Viscoelastic

    PMA: P880031 · Supplement: S009 · Decision Apr 9, 1996
    View on FDA
    Classifications
    1
    FEI Numbers
    27
    Registration Numbers
    27

    Basic Information

    Device Name
    Aid, Surgical, Viscoelastic
    Trade Name
    AMO(R) VITRAX(R) VISCOELASTIC SOLUTION
    PMA Number
    P880031
    Supplement Number
    S009
    Device Class
    FDA Class 3
    Product Code
    LZP
    Generic Name
    AID, SURGICAL, VISCOELASTIC
    Regulation Number
    886.4275
    Medical Specialty
    Ophthalmic
    Advisory Committee
    Ophthalmic
    Decision
    Approved
    Decision Code
    APPR
    Decision Date
    April 9, 1996
    Date Received
    October 17, 1995
    Supplement Type
    Normal 180 Day Track
    Supplement Reason
    Location Change - Manufacturer/Sterilizer/Packager/Supplier
    Expedited Review
    N

    Advisory Committee Statement

    NEW STERILIZATION SITE AT GRIFFITH MICRO SCIENCE IN GLEN FALLS, NEW YORK AND A NEW STERILIZATION PROCESS, 100% ETHYLENE OXIDE, FOR AMO VITRAX (SODIUM HYALURONATE) IN FINAL PACKAGING

    Classifications

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

    Product Code Device Name
    LZP Aid, Surgical, Viscoelastic