Search Filters

Search Results

Found 1 results

510(k) Data Aggregation

    K Number
    K041555
    Manufacturer
    Date Cleared
    2004-08-09

    (60 days)

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

    SECURVIEW DX SOFTCOPY WORKSTATION

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

    The Hologic SecurView DX device is intended for selection, display, manipulation, filming and media interchange of multi-modality images from a variety of different storage and printing devices using DICOM or similar interface standards.

    The device used with FDA cleared monitors may be used by a trained physician for display, manipulation and interpretation of lossless and on non-compressed or non-compressed mammographic images for screening and diagnostic mammography, as well as any other DICOM multi-modality image.

    Device Description

    The Hologic SecurView DX is mainly a software product. It is used for visualization and processing of radiology images. The SecurView DX is a multi-modality review workstation. It includes two high-resolution gray scale monitors (FDA cleared for Mammography), 3-button mouse, keyboard and workstation keypad. The software accepts images which have occurred. Image processing is external to the Presentation Specification in the DICOM Standard and the system allows for no compression at all when displaying mammography images.

    The minimum computer requirements are:

    Windows 2000® Operating System

    Intel CPU with a clock rate of 2.0 GHz or greater

    2.0 GB RAM or greater

    140 GB Hard drive or greater, operating at 160 Mbs or greater

    CD-ROM/R/RW, DVD+/-RW

    10/100 Base TX Network Interface

    AI/ML Overview

    The provided text is a 510(k) summary for the SecurView DX product. It describes the device's intended use and general information but does not contain any information regarding acceptance criteria, performance studies, sample sizes, ground truth establishment, or expert qualifications necessary to answer your request.

    The document is primarily a regulatory filing from the FDA, confirming the clearance of the device based on substantial equivalence to a predicate device. It details product classification, contact information, and indications for use.

    Therefore, I cannot provide the requested table and information based on the input text.

    Ask a Question

    Ask a specific question about this device

    Page 1 of 1