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510(k) Data Aggregation

    K Number
    K981574
    Manufacturer
    Date Cleared
    1998-07-06

    (63 days)

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

    For use in the daily cleaning, removing protein deposits, rinsing, chemical (not heat) disinfection and storage of soft (hydrophilic) contact lenses as recommended by your eye care practitioner.

    For use as a diluent for OPTI-FREE® SUPRACLENS® Daily Protein Remover.

    OPTI-FREE® Express® Multi-Purpose Solution can be used to dissolve OPTI-FREE® and OPTI-ZYME® Enzymatic Cleaning Tablets.

    Device Description

    OPTI-FREE® Express® Multi-Purpose Solution is a sterile, buffered, isotonic, aqueous solution containing sodium citrate and sodium chloride, with edetate disodium 0.05% and POLYQUAD® (polyquaternium-1) 0.001% as preservatives.

    AI/ML Overview

    The requested information is not available in the provided text. The document refers to the safety and effectiveness of the device, OPTI-FREE® Express® Multi-Purpose Solution, through a series of studies. However, it does not provide specific acceptance criteria or detailed study results in the format requested.

    The document states:

    • "A series of studies were conducted to demonstrate the ability of citrate in OPTI-FREE® Express Multi-Purpose Solution to continue to remove protein from lenses while they are being stored."
    • "Laboratory deposited and human worn lenses were divided and soaked in OPTI-FREE® Express® Multi-Purpose Solution and ReNu MultiPlus Multi-Purpose Solution."
    • "These studies demonstrate that OPTI-FREE® Express® Multi-Purpose Solution continues to remove protein while lenses are stored and that significantly more protein is removed during soaking in OPTI-FREE® Express® Multi-Purpose Solution than in ReNu MultiPlus Multi-Purpose Solution."

    This indicates that studies were performed, and they showed a positive outcome regarding protein removal. However, specific details such as:

    1. A table of acceptance criteria and the reported device performance
    2. Sample sized used for the test set and the data provenance
    3. Number of experts and their qualifications for ground truth
    4. Adjudication method
    5. Multi-reader multi-case (MRMC) comparative effectiveness study details
    6. Standalone (algorithm only) performance
    7. Type of ground truth used
    8. Sample size for the training set
    9. How the ground truth for the training set was established

    are not present in the provided text. The document is a 510(k) summary and an FDA clearance letter, which typically summarizes findings without detailing the full study methodology and results.

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