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510(k) Data Aggregation

    K Number
    K051469
    Date Cleared
    2005-09-28

    (117 days)

    Product Code
    Regulation Number
    868.5925
    Reference & Predicate Devices
    N/A
    Why did this record match?
    Device Name :

    CAREVENT ATV+ AND CAREVENT MRI

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

    The CAREvent ATV+ and CAREvent MRI are pneumatically powered, time cycled, intermittent, positive pressure automatic transport ventilator used to provide resuscitation and/or ventilatory support to a wide range of patients (from above 5 kg (11 lbs.) and higher) during transport.

    They are designed to be used by suitably trained medical personnel in the prehospital, Intra-hospital, inter-hospital and air ambulance settings.

    In addition CAREvent MRI is suitable for use in 1.5 - 3.0 Tesla MRI medical imaging suite environments, where ventilatory support may also be required during an MRI imaging procedure.

    The ventilator is suitable for use in:

    • · Pulmonary resuscitation during respiratory and/or cardiac arrest.
    • · Short term ventilatory support in the pre-hospital, Intra-hospital, inter-hospital and air ambulance transport of non-breathing patients.
    • · In addition CAREvent MRI only is suitable for use in 1.5 3.0 Tesla MRI medical imaging suite environments, where ventilatory support may also be required during an MRI imaging procedure.
    Device Description

    Not Found

    AI/ML Overview

    The provided text is a 510(k) premarket notification letter from the FDA regarding the CAREvent ATV+ and CAREvent MRI ventilators. It confirms substantial equivalence to predicate devices and outlines general regulatory requirements. However, it does not contain any information regarding acceptance criteria, device performance metrics, sample sizes, expert qualifications, adjudication methods, details of comparative effectiveness studies (MRMC), or standalone algorithm performance, or how ground truth was established for training or test sets.

    Therefore, I cannot fulfill the request for a table of acceptance criteria and reported device performance or other study details based solely on the provided text. The document is primarily an approval letter, not a detailed study report.

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