BEUDAMED
    FDA PMA FDA Class 3 Approved 🇺🇸 United States

    Intraocular Lens

    PMA: P930014 · Supplement: S103 · Decision Sep 21, 2017
    View on FDA
    Classifications
    1
    FEI Numbers
    59
    Registration Numbers
    59

    Basic Information

    Device Name
    Intraocular Lens
    Trade Name
    AcrySof IQ Tonic Lenses
    PMA Number
    P930014
    Supplement Number
    S103
    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
    September 21, 2017
    Date Received
    June 6, 2017
    Supplement Type
    Real-Time Process
    Supplement Reason
    Change Design/Components/Specifications/Material
    Expedited Review
    N

    Advisory Committee Statement

    Approval for the use of the Enhanced Dry NIMO Wavefront Measurement System for quality control inspection of optical performance for in situ spherical equivalent and cylindrical powers, image quality, spherical aberration and labeled axis of AcrySof® Toric Intraocular Lenses (IOLs), and spherical aberration and labeled axis of AcrySof® Multifocal and Multifocal-Toric Intraocular Lenses.

    Classifications

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

    Product Code Device Name
    HQL Intraocular Lens