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510(k) Data Aggregation

    K Number
    K970757
    Device Name
    FOTONA SKINSCAN
    Date Cleared
    1997-05-09

    (67 days)

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

    FOTONA SKINSCAN

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

    Not Found

    Device Description

    The Fotona Skinscan system is a microprocessor controlled device which generates precisely defined patterns on skin tissue in an automated sequence to increase uniformity and ease of treatment when used in conjunction with a host Skinlight system. The Fotona Skinscan system is designed as an accessory for use with the Fotona Skinlight laser system. Skinscan is functionally integrated to the host laser system. When the scanner head is attached to the articulated arm and the scanner cable is connected, the host laser system recognizes the presence and activation of the accessory and permits activation of the scanner specific modes which are programmed into the host at time of installation of the scanner accessory. In these modes scanner settings can be selected from an easy-toread menu. When the operator reverts to use of the standard dermatological handpiece, these settings are not accessible. When the scanner is connected and a scanner sub-menu is selected the system automatically initiates for scanner operation. The Skinscan system is designed with 3 major sub-systems a) A scanner handpiece comprising smoke evacuation components and distance gauge components. b) A scanner head, containing scanning mirrors and imaging optics. c) An electronic control hox containing scanning mirror control and laser interface circuitry.

    AI/ML Overview

    The provided text describes a medical device called the Fotona Skinscan system, an accessory for the Fotona Skinlight laser system. However, the text does not contain any information about acceptance criteria, device performance studies, sample sizes, expert qualifications, or ground truth methodologies.

    Therefore, I cannot fulfill your request for a table of acceptance criteria, study details, or information about MRMC studies, standalone performance, or training set specifics based on the provided input.

    The text focuses solely on:

    • Description of the device: Its components, function as an accessory to the Skinlight laser, and how it integrates with the host system.
    • Claim of substantial equivalence: Comparing it to the Coherent CPG system and stating that it raises no new questions of safety or effectiveness.
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