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510(k) Data Aggregation

    K Number
    K992955
    Device Name
    XPLORER 1000
    Date Cleared
    2000-06-02

    (275 days)

    Product Code
    Regulation Number
    892.1680
    Reference & Predicate Devices
    Why did this record match?
    Reference Devices :

    K974863

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

    Intended for use in general human radiography imaging similar to the optically coupled CCD based device cleared under 510(k) number K974863. Not to be used for mammography.

    Device Description

    The Xplorer 1000 is an optical based digital x-ray imager. It works by converting incident x-ray energy to visible light by use of fluorescent screen. The visible light is deflected by a mirror to a high resolution CCD camera that produces a digital image. The device trigger mechanism ensures that image is captured when the x-ray beam is turned on. The device does not require any connection to the x-ray generator.

    AI/ML Overview

    Here's a breakdown of the acceptance criteria and study as described in the provided documents for the Xplorer 1000 Digital X-ray Imager:

    Acceptance Criteria and Reported Device Performance

    The core acceptance criterion for the Xplorer 1000 was to demonstrate equivalence to its predicate devices: the IMIX DIGITAL THORAX SYSTEM (K974863) and conventional radiographic film (21 CFR 892.1840). This equivalence was assessed in terms of intended use and radiographic performance.

    Table of Acceptance Criteria and Reported Device Performance:

    Acceptance Criteria Category/MeasureAcceptance Criteria (Implicit for Predicate Equivalence)Reported Xplorer 1000 Performance
    Intended UseGeneral human radiography (same as predicates)General human radiography
    Radiographic Performance
    Spatial Resolution (microns at 100% MTF)At least 200 microns (IMIX) or
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