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510(k) Data Aggregation

    K Number
    K173762
    Date Cleared
    2018-07-18

    (219 days)

    Product Code
    Regulation Number
    870.1200
    Reference & Predicate Devices
    Predicate For
    N/A
    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
    Intended Use

    AngioDynamics Angiographic Catheters are for use where angiographic diagnosis is indicated.

    Device Description

    AngioDynamics Angiographic Catheters are sterile, single use, disposable devices designed to deliver radiopaque contrast media to selected sites in the vascular system. AngioDynamics Soft-Vu and Mariner Catheters come in the following sizes/structures:

    Soft-VuMariner
    French Size4F, 5F, 6F4F, 5F
    ShaftBraided and Non-BraidedBraided and Non-Braided
    TipNon-BraidedNon-Braided
    CoatingNon-CoatedCoated
    Lengths25cm - 150cm25cm - 150cm

    The only change presented in this 510(k) submission is a change to the colorant and the addition of heat and light stabilizers to the braided catheter shaft.

    AI/ML Overview

    The provided text is a 510(k) summary for AngioDynamics Angiographic Catheters. This document details the process for obtaining substantial equivalence for a medical device but does not contain information about the acceptance criteria or a study proving the device meets those criteria in the context of a diagnostic algorithm or AI/ML model.

    The "performance data" mentioned in section I only refers to non-clinical performance and material testing for the catheter itself (e.g., static pressure, tensile strength, biocompatibility), not a study assessing the diagnostic performance of software or an algorithm.

    Therefore, I cannot extract the requested information as it is not present in the provided text. The document is about a physical medical device (catheter), not a diagnostic algorithm or AI/ML device.

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