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510(k) Data Aggregation

    K Number
    K972921
    Date Cleared
    1998-01-06

    (151 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

    Intraoral dental x-ray machine, wall mounted system that produces x-rays and is intended for dental radiographic examination and diagnosis of diseases of the teeth, jaw, and oral structures.

    Device Description

    Sanko dental intaoral x-ray series 70 model_W1070-P

    AI/ML Overview

    I apologize, but the provided text from the FDA 510(k) K972921 for the Sanko Dental Intraoral X-Ray Series 70 Model W1070-P does not contain any information regarding acceptance criteria, device performance metrics, or study details as outlined in your request.

    The document is a clearance letter stating that the device is substantially equivalent to a pre-amendment device and outlines regulatory compliance information and contact details. It does not include:

    • A table of acceptance criteria or reported device performance.
    • Information about sample sizes for test or training sets.
    • Details on expert involvement, adjudication methods, or ground truth establishment.
    • Any mention of multi-reader multi-case (MRMC) studies or standalone algorithm performance.

    Therefore, I cannot fulfill your request to describe the acceptance criteria and the study that proves the device meets them based on the provided text.

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