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510(k) Data Aggregation

    K Number
    K253304

    Validate with FDA (Live)

    Date Cleared
    2025-11-25

    (57 days)

    Product Code
    Regulation Number
    878.4810
    Age Range
    All
    Reference & Predicate Devices
    Predicate For
    N/A
    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticPediatricDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
    Intended Use

    The IPL Hair Removal Device is an over-the-counter device intended for removal of unwanted body and/ or facial hair.

    Device Description

    IPL Hair Removal Device, is an over-the-counter, home-use device for unwanted hair removing by using Intense Pulsed Light (IPL), and it has been designed eight models with the same IPL technology for hair removal, which is model: KA-10, KA-11, KA-11C, KA-11D, KA-18, KA-20, KA-21, KA-21C. The device works below the skin's surface and does not involve any cutting or pulling, removing hair growth with minimal pain.

    The device is only powered by the external power adapter and its IPL emission activation is by finger switch or auto flash mode.

    The IPL Hair Removal Device has an irreplaceable flash window and it can cover an area of 3.0cm² for model KA-10, KA-11, KA-11C, KA-11D, and 3.3cm² for model KA-18, KA-20, KA-21, KA-21C, which is suitable for multiple hair removal areas, such as upper lip, armpit, bikini line, arms, legs, etc.

    The device contains a skin sensor to detect appropriate skin contact, if the flash window is not in full contact with the skin, the device cannot emit the treatment light pulses. Besides, the IPL Hair Removal Device has the sapphire cooling function (Model: KA-18, KA-20, KA-21) and ice cooling function (Model: KA-10, KA-11, KA-11C, KA-11D), which will be activated throughout the whole hair removal process to cool down the treatment area's temperature and provide the user with a better using experience.

    AI/ML Overview

    N/A

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    K Number
    K232056

    Validate with FDA (Live)

    Date Cleared
    2023-10-06

    (87 days)

    Product Code
    Regulation Number
    878.4810
    Age Range
    All
    Reference & Predicate Devices
    Predicate For
    N/A
    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticPediatricDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
    Intended Use

    The IPL Hair Removal Device is an over-the-counter device intended for removal of unwanted body and/ or facial hair.

    Device Description

    IPL Hair Removal Device (Model: PB1, PB2, PB3, PB4, TM002), is an over-the-counter, homeuse and personal device for hair reduction based on Intense Pulsed Light (IPL). It works below the skin's surface and does not involve any cutting or pulling, reducing hair growth with minimal pain. The indications for use, performance, structure design and operation of these five models of the device are basically the same, there is only a minor difference in appearance and physical dimension. The device is only powered by the external power adapter and its IPL emission activation is by finger switch. This product is equipped with a skin sensor to detect appropriate skin contact, if the flash window of the device is not in full contact with the skin, the device cannot emit the treatment light pulses.

    AI/ML Overview

    The provided text describes the FDA 510(k) clearance for an IPL Hair Removal Device. However, it does not contain the information necessary to describe acceptance criteria for an AI/CADe device, nor a study proving it meets those criteria.

    The document discusses:

    • The FDA clearance process for a medical device (specifically, an IPL hair removal device).
    • Comparison of the device to predicate devices based on technical specifications (e.g., energy density, wavelength, power supply).
    • Non-clinical performance data, primarily focusing on safety testing such as biocompatibility, electrical safety, electromagnetic compatibility (EMC), eye safety, software verification and validation, and usability.

    There is no mention of an AI/CADe component in this device, nor any study or data related to diagnostic performance, ground truth, expert readers, or statistical measures like sensitivity, specificity, or AUC.

    Therefore, I cannot provide the requested information for acceptance criteria and a study proving an AI/CADe device meets those criteria based solely on the provided text. The document pertains to a physical IPL hair removal device and its safety/performance testing, not an AI-powered diagnostic tool.

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