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510(k) Data Aggregation

    K Number
    K991021
    Date Cleared
    1999-06-23

    (86 days)

    Product Code
    Regulation Number
    872.4850
    Panel
    Dental
    Reference & Predicate Devices
    N/A
    Why did this record match?
    Device Name :

    SONIC SCALER WITH FIBER OPTIC, MODEL NAS-L, SONIC SCALER WITHOUT FIBER OPTIC, MODEL NAS-NL

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

    This device, an air-powered, fiber optic, swivel air scaler, is intended for use to remove calculus deposits and stains from a tooth, as done in normal dental scaling operation . The device uses controlled water spray and an appropriate scaling tip to wash away removed calculus and stains.

    Device Description

    air-powered, fiber optic, swivel air scaler

    AI/ML Overview

    Unfortunately, the provided document is a 510(k) clearance letter from the FDA for a "Sonic Scaler with Fiber Optic." This type of document primarily confirms that the device is substantially equivalent to existing devices and can be marketed.

    It does NOT contain the detailed information required to answer your questions about acceptance criteria and a study proving the device meets those criteria.

    Specifically, the document does not include:

    • A table of acceptance criteria or reported device performance.
    • Information about sample sizes, data provenance, or expert qualifications for a test set.
    • Details on adjudication methods, MRMC studies, or standalone performance.
    • The type of ground truth used or information about a training set.

    To obtain this information, you would typically need to refer to the device's 510(k) submission summary, engineering reports, or peer-reviewed studies related to the device, which are not part of this FDA clearance letter.

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