Search Filters

Search Results

Found 1 results

510(k) Data Aggregation

    K Number
    K192908
    Date Cleared
    2019-11-14

    (30 days)

    Product Code
    Regulation Number
    876.1500
    Reference & Predicate Devices
    Predicate For
    N/A
    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
    Intended Use

    Used for collection of cells in the biliary system.

    Device Description

    The subject devices, the Fusion Cytology Brush and CytoMax II Double Lumen Cytology Brush, consist of a nylon brush on a stainless-steel drive wire with a stainless-steel tip, a double lumen catheter with ink markings, radiopaque markers, wire guide access via a wire guide hub or and IDE port, a detachable extension line with a luer lock for optional flushing of the wire guide hub and a pin-vise handle.

    The Fusion Cytology Brush and CytoMax II Double Lumen Cytology Brushes are used by passing the device through an endoscope over a prepositioned wire guide to a target location. The cytology brush is located at the distal end (patient contacting) of the device with the pin vise handle located at the proximal end (non-patient contacting). The handle is actuated by pushing the pin vise handle forward to extend the cytology brush and then pulling backward to retract the brush.

    AI/ML Overview

    The provided text is a 510(k) summary for the Fusion Cytology Brush and CytoMax II Double Lumen Cytology Brush. This document focuses on demonstrating substantial equivalence to previously cleared predicate devices after a design modification. It does not describe an AI medical device, nor does it contain information about acceptance criteria for an AI model, a study proving an AI device meets acceptance criteria, sample sizes for test or training sets for AI, expert involvement for AI ground truth, or MRMC studies.

    Therefore, I cannot fulfill your request for information about acceptance criteria and studies related to an AI device based on this input.

    The document discusses non-clinical bench testing to ensure the modified devices meet performance requirements and function as intended, specifically:

    • Tensile Strength Testing: Assesses the strength of the device.
    • Tensile Strength of Handle: Evaluates the handle's ability to withstand pulling forces.

    These tests are to ensure the physical integrity and functionality of the cytology brushes themselves, not the performance of an AI algorithm.

    Ask a Question

    Ask a specific question about this device

    Page 1 of 1