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510(k) Data Aggregation

    K Number
    K163552
    Manufacturer
    Date Cleared
    2017-03-03

    (74 days)

    Product Code
    Regulation Number
    878.4810
    Reference & Predicate Devices
    N/A
    Why did this record match?
    Device Name :

    iPulse SmoothSkin BARE Hair Removal Device

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

    The iPulse SmoothSkin BARE Hair Removal System is indicated for the removal of unwanted hair. The iPulse SmoothSkin BARE is also indicated for the permanent reduction in hair regrowth, defined as the long-term, stable reduction in the number of hairs regrowing when measured at 6, 9 and 12 months affer the completion of a treatment regime.

    Device Description

    Not Found

    AI/ML Overview

    The provided text is a 510(k) premarket notification clearance letter from the FDA for the "iPulse SmoothSkin Bare Hair Removal System." This document primarily focuses on regulatory approval and does not contain the detailed study information about acceptance criteria and device performance that you are requesting.

    Therefore, I cannot fulfill your request using only the information provided. The document states that the FDA reviewed the premarket notification and determined the device is substantially equivalent to legally marketed predicate devices, but it does not include the specifics of the clinical study, performance metrics, ground truth establishment, or expert involvement.

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