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510(k) Data Aggregation

    K Number
    K022621
    Date Cleared
    2002-09-04

    (28 days)

    Product Code
    Regulation Number
    870.1200
    Reference & Predicate Devices
    Why did this record match?
    Device Name :

    BOSTON SCIENTIFIC IMAGER II 4F SELECTIVE ANGIOGRAPHIC CATHETER

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

    The IMAGER™ II Angiographic Catheters are designed to provide a pathway for delivering contrast media to selected sites in the vascular system.

    Device Description

    The IMAGER™II Angiographic Catheters are designed to provide a pathway for delivering contrast media to selected sites in the vascular system. The IMAGER™ Angiographic Catheters are sterile, single-use diagnostic intravascular catheters and are available in a variety of flush and selective curve styles with lengths of 40 cm, 65 cm, 90cm and 100 cm. The distal segment of the catheter is radiopaque to aid in visualization of the device under fluoroscopy.

    AI/ML Overview

    This document describes the Boston Scientific Imager™ II 4F Selective Angiographic Catheter, a diagnostic intravascular catheter. The provided text outlines its intended use and demonstrates its substantial equivalence to a predicate device through non-clinical testing. However, it does not contain information about an AI/ML powered device or any study that measures device performance against acceptance criteria in the context of an AI/ML system.

    Therefore, I cannot fulfill your request for:

    • A table of acceptance criteria and the reported device performance for an AI/ML device.
    • Sample size and data provenance for a test set for an AI/ML device.
    • Number and qualifications of experts for ground truth for an AI/ML device.
    • Adjudication method for a test set for an AI/ML device.
    • Multi-reader multi-case (MRMC) comparative effectiveness study information for an AI/ML device.
    • Standalone performance information for an AI/ML device.
    • Type of ground truth used for an AI/ML device.
    • Sample size and ground truth establishment for a training set for an AI/ML device.

    The document describes a traditional medical device (catheter) and its regulatory clearance process based on substantial equivalence to existing predicate devices, primarily through mechanical and functional performance testing.

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