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510(k) Data Aggregation

    K Number
    K034059
    Manufacturer
    Date Cleared
    2004-03-09

    (69 days)

    Product Code
    Regulation Number
    892.2050
    Reference & Predicate Devices
    Why did this record match?
    Device Name :

    SECTRA ANGIOGRAPHY PACKAGE AND SECTRA CARDIOLOGY PACKAGE

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

    The Sectra Angiography and Cardiology Package provides quantitative and reproducible information regarding the calculated dimensions of arterial segments, and quantitative information regarding the calculated dimensions and calculated performance characteristics of the left vertical of the heart, imaged during angiographic x-ray procedures typically performed in cath labs.

    This information is suitable for use in the following applications:

    1. Scientific and research studies, assessing the angiographic condition of patients and the result of device and drug therapeutics,
    2. Review and analysis of patient angiographic imaging records, providing additional information to physicians and administrators.
    Device Description

    Sectra Angiography and Cardiology Package is intended to support radiologists and cardiologists in the diagnostic process to quantify findings. The device has functionality for quantitative analysis of the arteriograms (QCA and QVA) and quantitative analysis of the left ventricular angiographic images (LVA). Measurements can be applied on angiographic images.

    AI/ML Overview

    The provided text does not contain acceptance criteria for device performance or a study demonstrating that the device meets such criteria.

    The document is a 510(k) summary for the Sectra Angiography and Cardiology Package, which focuses on demonstrating substantial equivalence to predicate devices rather than providing detailed performance studies or specific acceptance criteria.

    The "Performance Data" section merely states: "The subject device is developed according to ISO 9001:2000 and complies with ACR/NEMA Digital Imaging Communications in Medicine version 3.0." This indicates compliance with quality management systems and communication standards, not a clinical performance study with acceptance criteria.

    Therefore, I cannot populate the requested table or answer most of the questions, as the information is not present in the provided text.

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