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510(k) Data Aggregation

    K Number
    K964049
    Date Cleared
    1997-01-06

    (89 days)

    Product Code
    Regulation Number
    880.5200
    Reference & Predicate Devices
    N/A
    Why did this record match?
    Device Name :

    FIRST MIDCATH CATHETER WITH DUAL LUMENS

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

    to provide access to the vascular system to sample blood or administer drug solutions, blood products, or other fluids intravenously.

    Device Description

    The subject catheter is a long term, single use, dual lumen, intravascular catheter of various French sizes and lengths which is designed to provide access to large veins such as the baslic or cephalic veins. It is inserted into the vascular system through a spittable introducer catheter.

    AI/ML Overview

    This submission describes a medical device, specifically a "Midline Catheter with Dual Lumens," and seeks to establish its substantial equivalence to a predicate device. However, the provided text does not contain the information necessary to describe acceptance criteria or a study proving the device meets those criteria in the context of device performance,
    such as accuracy or efficacy. The document focuses on regulatory identification and comparison to a predicate device based on material and design, not on performance metrics.

    Therefore, I cannot generate the requested table and details about a performance study. The provided text is insufficient for this purpose.

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