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510(k) Data Aggregation

    K Number
    K041580
    Device Name
    IMAGERAYI
    Manufacturer
    Date Cleared
    2004-06-29

    (15 days)

    Product Code
    Regulation Number
    872.1800
    Reference & Predicate Devices
    N/A
    Predicate For
    N/A
    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
    Intended Use

    The digital x-ray sensor system, ImageRAYi, of Dental Systems, Inc. which is a subsidiary of Henry Schein Company, Inc., and its related components are used to provide instant x-ray is a suosimar of Homan oral tissue (dentin). The digital x-ray sensor system, ImageRAYi, replaces standard intraoral x-ray film and uses the same x-ray source.

    Device Description

    digital x-ray sensor system

    AI/ML Overview

    This document is a 510(k) premarket notification letter from the FDA to Dentrix Dental Systems, Inc. regarding their ImageRAYi device. It states that the device is substantially equivalent to legally marketed predicate devices.

    However, this document does not contain information about acceptance criteria, device performance studies, sample sizes, expert qualifications, adjudication methods, MRMC studies, standalone performance, ground truth types, or training set details.

    The letter is a regulatory approval, not a scientific report detailing the clinical validation or performance metrics of the device. It indicates that the device has met the regulatory hurdle of substantial equivalence, which means it is as safe and effective as a legally marketed predicate device. To find the information requested, one would typically need to refer to the 510(k) submission itself, or any associated clinical or performance studies included within that submission, rather than just the FDA's decision letter.

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