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510(k) Data Aggregation

    K Number
    K974238
    Date Cleared
    1998-02-04

    (84 days)

    Product Code
    Regulation Number
    872.6640
    Panel
    Dental
    Reference & Predicate Devices
    N/A
    Why did this record match?
    Device Name :

    DENTAL TRAY, STERILE, DISPOSABLE

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

    Trinity's Dental Tray is a sterile prepackaged disposable unit. It contains the gowns, table cover, mayo stand cover, OR towels, bowl, medicine cup, sponges, scalpels, tongue depressor, foam tray, Yankauer, suction tubing, and towels necessary for the performance of basic dental procedures, including but not limited to general cleaning, cavity filling, root canal, and tooth removal.

    Device Description

    Trinity's Dental Tray is a sterile prepackaged disposable unit. It contains the gowns, table cover, mayo stand cover, OR towels, bowl, medicine cup, sponges, scalpels, tongue depressor, foam tray, Yankauer, suction tubing, and towels necessary for the performance of basic dental procedures, including but not limited to general cleaning, cavity filling, root canal, and tooth removal.

    AI/ML Overview

    The provided document is a 510(k) premarket notification letter from the FDA for a "Dental Tray, Sterile, Disposable" manufactured by Trinity Laboratories, Incorporated.

    This document does not contain any information regarding acceptance criteria, device performance studies, or details about artificial intelligence (AI) performance. The letter is solely an FDA notification of substantial equivalence for a medical device.

    Therefore, I cannot provide the requested information. The document does not describe:

    • A table of acceptance criteria and reported device performance.
    • Sample sizes, data provenance, or the number/qualifications of experts for a test set.
    • Adjudication methods.
    • Multi-reader multi-case (MRMC) comparative effectiveness studies or effect sizes for AI assistance.
    • Standalone algorithm performance.
    • Type of ground truth used.
    • Sample size for a training set or how ground truth for a training set was established.

    This document is a regulatory approval for a physical medical device (a sterile, disposable dental tray) and not a submission or report for an AI/software as a medical device.

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