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510(k) Data Aggregation

    K Number
    K221481
    Device Name
    NeutrArt
    Date Cleared
    2022-09-23

    (123 days)

    Product Code
    Regulation Number
    880.5440
    Reference & Predicate Devices
    N/A
    Predicate For
    N/A
    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
    Intended Use

    Extension sets are for administering fluids from container to a patient's vascular system through a vascular access device.

    Needleless valve allows the user to add medication into the without the use of a needle.

    Power Injection Rating and Flowrate (400 psi and 10 mL/sec).

    Device Description

    Not Found

    AI/ML Overview

    I am sorry, but the provided text does not contain information about acceptance criteria, device performance, or any study details that would enable me to answer your request. The document is an FDA 510(k) clearance letter for a medical device called "NeutrArt," an intravascular administration set. It discusses regulatory matters, indications for use, and administrative information, but it does not include clinical study data or performance metrics.

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    K Number
    K201872
    Device Name
    NeutrArt
    Date Cleared
    2021-01-05

    (182 days)

    Product Code
    Regulation Number
    880.5440
    Reference & Predicate Devices
    N/A
    Predicate For
    N/A
    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
    Intended Use

    Extension sets are for administering fluids from container to a patient's vascular system through a vascular access device.

    Stopcocks are intended for use to change the direction of fluids through a tubing set.

    Needleless valve allows the user to add medication into the without the use of a needle.

    Device Description

    Not Found

    AI/ML Overview

    This document is a 510(k) clearance letter for the NeutrArt device, which is an intravascular administration set. It provides regulatory information and indicates that the device has been found substantially equivalent to predicate devices. However, this document does not contain any information about acceptance criteria, device performance studies, sample sizes, ground truth establishment, or expert involvement as requested in your prompt.

    Therefore, I cannot provide a response based on the input text. Please provide a document that contains information about the device's technical specifications, performance studies, and validation processes.

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