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510(k) Data Aggregation

    K Number
    K080638
    Device Name
    CLARO
    Date Cleared
    2008-09-17

    (195 days)

    Product Code
    Regulation Number
    878.4810
    Reference & Predicate Devices
    Predicate For
    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
    Intended Use

    The CLARO is indicated for the treatment of individual acne pimples in persons with mild to moderate inflammatory acne.

    Device Description

    The CLARO is a portable handheld device that uses light energy from the blue to infra-red spectrum emitted by a Xenon flash lamp. The device is powered by a rechargeable battery. CLARO is intended to be a prescription device which will be used both in the doctor's office and in the home environment for the treamment of mild to moderate acne.

    AI/ML Overview

    The provided text, a 510(k) summary for the CLARO device, does not contain specific acceptance criteria or details of a study proving the device meets particular performance metrics.

    Instead, it states:

    "Performance testing will be performed which will demonstrate compliance with IEC 60601-1-1 and IEC 60601-1-2. Testing was submitted which showed that the user was able to use the device in the home-use environment."

    This indicates that general safety and essential performance standards (IEC 60601-1-1 and -1-2) would be addressed, and a user study demonstrated home-use feasibility. However, no specific performance criteria related to acne treatment efficacy, clinical outcomes, or comparative performance are detailed, nor are the results of any such study presented in this document.

    Therefore, I cannot provide the requested information. The document focuses on regulatory submission and substantial equivalence to predicate devices, not on detailed performance study results against specific acceptance criteria for efficacy.

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