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510(k) Data Aggregation

    K Number
    K955886
    Manufacturer
    Date Cleared
    1996-03-11

    (74 days)

    Product Code
    Regulation Number
    870.1250
    Reference & Predicate Devices
    N/A
    Why did this record match?
    Device Name :

    MEGA PTA BALLOON CATHETER

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

    The Cordis Mega PTA Balloon Catheters are designed for dilatation of stenotic lesions within the peripheral vessels.

    Device Description

    Mega catheters have a coaxial design (tube within a tube) with a balloon on the distal tip. Two (2) lumens, an inner and outer lumen, are split on the proximal end by a Y-shaped one piece hub. The inner lumen (denoted by "thru") molded into the hub) is used for contrast medium or saline injections and guidewire insertion (maximum guidewire diameter is 0.018"). The outer lumen (denoted by "balloon" molded into the hub) is used for inflation and deflation of the balloon. Two (2) radiopaque marker bands placed within the balloon working length aid the physician in proper balloon placement.

    AI/ML Overview

    The provided text is a summary of substantial equivalence for a medical device (Cordis Mega PTA Balloon Catheter) and does not contain any information about acceptance criteria or a study proving device performance against such criteria. The document is a K95 submission (a premarket notification for a Class II medical device) and focuses on demonstrating substantial equivalence to predicate devices, rather than establishing performance against specific acceptance criteria through a clinical study involving AI or human readers.

    Therefore, I cannot provide the requested information based on the input text. The questions posed in your request are typically relevant to the evaluation of AI/ML-enabled medical devices or clinical studies, which is not the subject of this document.

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