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510(k) Data Aggregation

    K Number
    K162597

    Validate with FDA (Live)

    Date Cleared
    2016-10-19

    (30 days)

    Product Code
    Regulation Number
    886.5928
    Reference & Predicate Devices
    Predicate For
    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
    Intended Use

    For use in simultaneous cleaning, daily protein removal, disinfecting, and storage of soft (hydrophilic) contact lenses (including silicone hydrogel lenses) or rigid gas permeable (fluoro silicone acrylate and silicone acrylate) contact lenses as recommended by your eye care practitioner.

    Device Description

    The two color AOCup Lens Case with AODisc is equivalent to the predicate device except modifications of colorants and minor modifications to basket geometry.

    It is a specialized lens case consisting of a transparent cup with a connected unit of screw cap, lens holders (baskets) and platinum-coated neutralization disc. The platinum catalyst coating and shape of the plastic disc are designed to effectively neutralize the strong oxidizing agent hydrogen peroxide to harmless water and oxygen gas.

    The modifications of colorants and basket geometry do not change any indications for use nor the basic technical principle of the device functions.

    AI/ML Overview

    The provided text is a 510(k) Premarket Notification from the FDA regarding a contact lens care product. It does not contain information about an AI-powered device or a study involving acceptance criteria, expert ground truth, multi-reader multi-case studies, or training/test set details as requested in your prompt.

    Therefore, I cannot provide the information you asked for based on the input text. The document is a regulatory filing for a physical medical device (contact lens case and solution), not a software or AI-based device that would require the type of performance evaluation details you've described.

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