Search Filters

Search Results

Found 1 results

510(k) Data Aggregation

    K Number
    K031638
    Date Cleared
    2003-07-21

    (55 days)

    Product Code
    Regulation Number
    892.2050
    Reference & Predicate Devices
    Predicate For
    N/A
    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
    Intended Use

    The CVIEW™ is a high performance, digital, cardiac image viewer. The System supports DICOM 3.x and higher cardiac and angio images and displays them in their original dynamic mode. The CVIEW accepts images from DICOM 3.x CDs or can be configured to read DICOM 3 images from a DICOM Archive Server. The CVIEW allows immediate playback of images from any patient stored on the system and burning CDs in the DICOM part 10 - file format.

    It represents the next generation in network cardiac review systems. Features include 1024 viewing, security, report generation, multi-modality viewing, databasing as well as instant access to hundreds of cases on-line or thousands through the network.

    Device Description

    Cardio Vascular Information Enhanced Workstation™ (CVIEW)™ is a viewing stations for Cath, Echo and Angio case studies, represent the next generation in network cardiac review systems. Features include 1024 viewing, security, report generation, multi-modality viewing, databasing as well as instant access to hundreds of cases on-line or thousands through the network.

    AI/ML Overview

    This 510(k) summary explicitly states that clinical performance data was "Not required for determination of substantial equivalence for this type and class of device." Therefore, there is no study provided within this document that describes acceptance criteria and proves the device meets them.

    The Cardio Vascular Information Enhanced Workstation (CVIEW)™ was approved based on its substantial equivalence to predicate devices, meaning its intended use and technological characteristics were similar or equivalent to already legally marketed devices.

    As a result, I cannot provide the requested information for acceptance criteria and a study proving their fulfillment as this information is not present in the provided document. All the numbered points in your request relate to details of a clinical study, which was not performed for this 510(k) clearance.

    Ask a Question

    Ask a specific question about this device

    Page 1 of 1