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510(k) Data Aggregation

    K Number
    K190938
    Date Cleared
    2019-06-26

    (77 days)

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

    Phototherapy Systems use of the red, blue and infrared regions of the spectrum is intended to emit energy to treat dermatological conditions.

    The blue light (415nm wavelength) is generally indicated to treat dermatological conditions and specifically indicated to treat moderate inflammatory acne vulgaris

    The red light (630mm wavelength) is generally indicated to treatment of superficial, benign vascular, and pigmented lesions

    The infrared light (835nm wavelength) is generally use for the temporary relief of minor muscle and joint pain, atthritis and muscle spasm; relieving stiffness; promoting the relaxation of muscle tissue; and to temporarily increase local blood circulation where applied.

    Device Description

    The Phototherapy Systems HS-770 is a vertical device which uses specific wavelengths of light, produced by LEDs (Light emitting diodes), to manage aesthetic conditions. The device produces light in the red light region of the spectrum (630±15nm), in the blue light regions of the light spectrum (415±15nm) and infrared light region of light spectrum (835±15nm). Three or four sets of LEDs panels are available for the device.

    AI/ML Overview

    The provided text is a 510(k) Summary for a Phototherapy System, which details its specifications and compares it to a predicate device. It explicitly states that clinical testing was not applicable or performed for this submission to establish substantial equivalence.

    Therefore, the document does not contain any information regarding acceptance criteria studies, device performance metrics against such criteria, sample sizes for test sets, data provenance, expert qualifications, adjudication methods, MRMC studies, standalone algorithm performance, or details about training sets.

    The information provided only covers non-clinical testing for electrical safety and electromagnetic compatibility to demonstrate compliance with recognized standards.

    Based on the provided text, I cannot answer the questions about acceptance criteria and the study that proves the device meets them because the document states "Clinical Testing: It is not applicable."

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