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510(k) Data Aggregation

    K Number
    K110246
    Date Cleared
    2011-11-04

    (281 days)

    Product Code
    Regulation Number
    868.5260
    Reference & Predicate Devices
    N/A
    Predicate For
    N/A
    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
    Intended Use

    1 The Medisize Red devices with catheter mount are breathing circuit bacterial/viral filters, which are intended to remove microbiological and particulate matter from the gases in the breathing circuit.

    2 The Medisize Blue devices with catheter mount are Filter/HME's. These devices are intended to remove microbiological and particulate matter from the gases in the breathing circuit and at the same time the device is intended to be positioned over a tracheotomy or tracheal tube to warm and humidify by passive means gases breathed in by patient during anesthesia and ventilator care.

    Device Description

    Not Found

    AI/ML Overview

    This document is a 510(k) clearance letter from the FDA for two medical devices: "Medisize Red Devices with Catheter Mount" and "Medisize Blue Devices with Catheter Mount." These devices are classified as Breathing Circuit Bacterial Filters. The letter confirms that the devices are substantially equivalent to legally marketed predicate devices.

    However, the provided document does not contain any information about acceptance criteria, device performance described in a study, sample sizes, data provenance, expert qualifications, adjudication methods, MRMC studies, standalone performance, ground truth types, or training set details.

    The document is a regulatory approval letter and does not include the detailed technical study data that would typically be found in a 510(k) submission's performance section. Therefore, I cannot generate the requested table and information based on the text provided.

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