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510(k) Data Aggregation

    K Number
    K964056
    Manufacturer
    Date Cleared
    1997-10-10

    (366 days)

    Product Code
    Regulation Number
    868.5800
    Reference & Predicate Devices
    Predicate For
    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
    Intended Use

    The Rusch UltraTracheoflex®Tracheoflex® Tracheostomy Tube Kits are intended for use in airway management of tracheostomized patients.

    Device Description

    Tracheoflex® Fenestrated Tracheostomy Set-Cuffed, Tracheoflex® The Ultra Tracheostomy Set-Uncuffed, Tracheoflex® Fenestrated Tracheostomy Set-Uncuffed, are sterile, disposable, single use cuffed, or uncuffed fenestrated fixed length fenestrated tracheostomy tubes with a fixed flange. The kit may include a radiopaque tube, a tube obturator, a cough cap, a 15 mm airway connector, phonation value, a sealing cap, exchangeable inner cannulas, and a neck band. The inner cannula will be also available as a separate item.

    AI/ML Overview

    The provided text describes medical device submission for tracheostomy tube kits, not an AI/ML device. Therefore, it does not contain information about acceptance criteria or study data for an AI/ML device.

    Specifically, the document states: "No clinical testing was completed." This directly indicates that no study was performed to assess the device's performance against specific acceptance criteria. The submission focuses on demonstrating substantial equivalence to already marketed devices based on features, materials, and dimensions.

    Therefore, I cannot provide the requested information.

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