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510(k) Data Aggregation

    K Number
    K053046
    Manufacturer
    Date Cleared
    2005-11-08

    (11 days)

    Product Code
    Regulation Number
    892.1750
    Reference & Predicate Devices
    N/A
    Why did this record match?
    Device Name :

    ILUMA ORTHOCAT/DENTALCAT

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

    The IMTEC Imaging ILUMA™ OrthoCat™ and DentalCat™ are x-ray devices (cone beam computed tomography) that acquire a single 360° rotational sequence of the head and neck areas, including the ENT and dentomaxillofacial area for use in diagnostic support.

    Device Description

    x-ray devices (cone beam computed tomography) that acquire a single 360° rotational sequence

    AI/ML Overview

    The provided text is a 510(k) clearance letter from the FDA for the ILUMA OrthoCat/DentalCat device. This document primarily focuses on the regulatory approval process and does not contain the specific details about acceptance criteria, study design, or performance metrics that would typically be found in a study report or a more detailed section of a 510(k) submission.

    Therefore, I cannot extract the requested information regarding acceptance criteria and the study proving the device meets those criteria from the provided text. The document confirms that the device is substantially equivalent to a predicate device but does not elaborate on the specific performance studies conducted to demonstrate this equivalence in terms of detailed metrics, sample sizes, ground truth establishment, or expert reviews.

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