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510(k) Data Aggregation

    K Number
    K033333
    Date Cleared
    2003-11-14

    (29 days)

    Product Code
    Regulation Number
    876.5010
    Reference & Predicate Devices
    Why did this record match?
    Reference Devices :

    K962925

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

    These instruments have been designed to be used with Olympus endoscopes to inject contrast media into the biliary or pancreatic tract. They can also be used for retrieval of biliary or pancreatic stones.

    Device Description

    The subject device(s) is a balloon catheter that has a triple-lumen catheter and a multiple sizing balloon with pre-measured syringes, to be used in accordance with Intended use of the device. These functions ensure smoother passage of the guidewire and injection of the contrast media without removing the guidewire, and enable to inflate one balloon to 3 different sizes.

    AI/ML Overview

    The provided document, K033333, is a 510(k) premarket notification for a medical device: the Single Use 3-Lumen Balloon Catheter, Models B-230Q-A and B-230Q-B.

    This document does not contain any information regarding acceptance criteria or a study proving that the device meets such criteria. The 510(k) submission primarily focuses on demonstrating substantial equivalence to a predicate device (B-5/B-7 series Balloon Catheter K962925) based on intended use, method of operation, materials, and design, and explicitly states that no significant changes that could affect safety or effectiveness were made.

    Therefore, I cannot provide the requested information in the format specified because the document does not contain the necessary details about performance studies, sample sizes, ground truth establishment, or expert involvement.

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