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510(k) Data Aggregation

    K Number
    K180319
    Date Cleared
    2018-03-27

    (50 days)

    Product Code
    Regulation Number
    886.5918
    Reference & Predicate Devices
    Why did this record match?
    Device Name :

    Bausch + Lomb Boston Advance Cleaner, Bausch + Lomb Boston Advance Conditioning Solution

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
    Intended Use

    Boston ADVANCE Cleaner is indicated for use to clean fluoro silicone acrylate and silicone acrylate gas permeable contact lenses after each removal and before conditioning (wetting, soaking, disinfecting).

    Boston ADVANCE Conditioning Solution is indicated for wetting, disinfecting and soaking (after cleaning and rinsing) fluoro silicone acrylate and silicone acrylate gas permeable contact lenses.

    Device Description

    Boston ADVANCE Cleaner is a sterile, concentrated, homogeneous surfactant solution containing alkyl ether sulfate, ethoxylated alkyl phenol, tri-quaternary cocoa-based phospholipid and silica gel as cleaning agents; with titanium dioxide.

    Boston ADVANCE Conditioning Solution is a sterile, aqueous, buffered, slightly hypertonic solution containing a cationic cellulose derivative polymer, a cellulosic viscosifier, polyvinyl alcohol and a derivatized polyethylene glycol as wetting and cushioning agents; preserved with chlorhexidine gluconate (0.003%), polyaminopropyl biguanide (0.0005%) and edetate disodium (0.05%).

    AI/ML Overview

    The provided document is a 510(k) premarket notification for Bausch + Lomb Boston ADVANCE Cleaner and Conditioning Solution. It is not a document describing a medical imaging AI device or a study involving human readers and AI assistance.

    Therefore, none of the requested information regarding acceptance criteria, study design, sample sizes, expert qualifications, ground truth establishment, MRMC studies, or standalone algorithm performance can be extracted from this document.

    This document primarily focuses on demonstrating substantial equivalence of a modified contact lens care regimen (replacing water rinse with saline solution) to a previously cleared regimen, based on microbiology and lens compatibility testing, and re-using previously established biocompatibility and clinical data.

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