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510(k) Data Aggregation

    K Number
    K030235
    Manufacturer
    Date Cleared
    2003-04-23

    (90 days)

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

    F1 DIODE LASER SYSTEM

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

    The Device is indicated for hair removal and permanent hair reduction in dermatology and plastic surgery procedures.

    Device Description

    The F1 Diode Laser System delivers a pulsed infrared laser light at a wavelength of 810 nanometers. The laser consists of several interconnected sections: The cabinet which houses the laser diode, the power supply, the PC-104, and the microcontroller, the umbilical which houses the fiber optics delivery system, and the handpiece and the external TE chiller.

    AI/ML Overview

    This submission is a 510(k) premarket notification for the F1 Diode Laser System. The provided documents establish substantial equivalence to predicate devices based on intended use and technological characteristics. However, they do not contain information about specific acceptance criteria, device performance studies, sample sizes, ground truth establishment, or any details related to AI or MRMC studies.

    Therefore, I cannot fulfill the request to provide a table of acceptance criteria and reported device performance or details about the studies as such information is not present in the provided text.

    The closest information available is the claim that:

    • "The device, as designed, is as safe and effective as the predicate devices, and the device is substantially equivalent to the referenced predicate devices."
    • "The differences between the F1 Diode Laser System and the predicate devices cited do not raise any different questions regarding safety and effectiveness."

    This indicates a qualitative assessment of equivalence rather than a quantitative study with defined acceptance criteria and performance metrics.

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    K Number
    K004021
    Manufacturer
    Date Cleared
    2001-03-27

    (90 days)

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

    F1 DIODE LASER SYSTEM

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
    Intended Use
    Device Description
    AI/ML Overview
    Ask a Question

    Ask a specific question about this device

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