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510(k) Data Aggregation

    K Number
    K023964
    Manufacturer
    Date Cleared
    2002-12-23

    (24 days)

    Product Code
    Regulation Number
    868.5730
    Reference & Predicate Devices
    Why did this record match?
    Device Name :

    RUSCH MICROLARYNGEAL TUBE

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

    The Rüsch Microlaryngeal Tube is a sterile, single-use, oral/nasal tracheal tube intended to be used for airway management during laryngeal procedures.

    Device Description

    The Rüsch Microlaryngeal Tube will be offered in three (3) sizes - 4.0mm, 5.0mm and 6.0mm ID. The devices will have a low-pressure/high volume cuff, inflated via a luer activated valve. A pilot balloon will be provided to give a visual indication of cuff status. The Rüsch Microlaryngeal Tube consists of a clear, implant-tested tracheal tube with a radiopaque stripe. The main tube is graduated with multiple centimeter markings to facilitate determination of intubated length.

    AI/ML Overview

    The provided document is a 510(k) premarket notification for a medical device, the Rüsch Microlaryngeal Tube. It focuses on demonstrating substantial equivalence to pre-existing devices, rather than presenting a performance study with acceptance criteria in the context of an AI/ML powered device.

    Therefore, the requested information regarding acceptance criteria, study data, sample sizes, ground truth establishment, expert involvement, and MRMC studies for an AI/ML device is not available in this document.

    This document describes a traditional medical device (a tracheal tube) and uses substantial equivalence as its regulatory pathway, which involves comparing its design, materials, and intended use to legally marketed predicate devices. It does not involve any AI/ML components or associated performance studies.

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