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510(k) Data Aggregation

    K Number
    K031554
    Manufacturer
    Date Cleared
    2003-07-25

    (67 days)

    Product Code
    Regulation Number
    868.5830
    Reference & Predicate Devices
    Why did this record match?
    Device Name :

    S-1150 PLEUR-EVAC SAHARA PLUS CONTINUOUS REINFUSION AUTOTRANSFUSION SYSTEM

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

    The Pleur-evac Sahara Plus Continuous Reinfusion Autotransfusion System is indicated for use: AUTOTRANSFUSION 1) for the collection of autologous blood from the patient's pleural cavity or mediastinal area for reinfusion purposes in trauma and post operative situations CHEST DRAINAGE - 1) to evacuate air and/or fluid from the chest cavity or mediastrinum - 2) to help prevent air and/or fluid from reaccumulating in the chest cavity or mediastinum - 3) to help re-establish and maintain normal intrathoracic pressure gradients - 4) to facilitate complete lung re-expansion to restore normal breathing dynamic.

    Device Description

    The Pleur-evac Sahara Plus Continuous Reinfusion Autotransfusion System is a multi-chamber collection/reinfusion system. The Pleur-evac Sahara Plus Continuous Reinfusion Autotransfusion System is a sterile, single use devices intended for the collection of autologous blood (autotransfusion) and as chest drainage collection units.

    AI/ML Overview

    The provided text describes a 510(k) submission for the Pleur-evac® Sahara Plus Continuous Reinfusion Autotransfusion System. However, it does not contain any information about acceptance criteria, device performance studies, sample sizes, expert involvement, or ground truth establishment relevant to the request.

    The document confirms that this device is "substantially equivalent" to a previously marketed device (K963850) based on "a detailed device description, performance testing and conformance with consensus and voluntary performance standards." However, the details of these performance tests, including specific acceptance criteria and study results, are not elaborated upon in the provided sections.

    Therefore, I cannot fulfill the request for information regarding acceptance criteria and the study that proves the device meets them because the necessary details are absent from the provided text.

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