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510(k) Data Aggregation

    K Number
    K973289
    Device Name
    RE NU
    Date Cleared
    1999-02-09

    (525 days)

    Product Code
    Regulation Number
    872.6030
    Panel
    Dental
    Reference & Predicate Devices
    N/A
    Predicate For
    N/A
    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
    Intended Use

    For use by a dental professional for the purpose of cleaning teeth.

    Device Description

    RE NU Prophy Paste

    AI/ML Overview

    The provided document is a 510(k) clearance letter from the FDA for a device named "RE NU Prophy Paste". This type of letter indicates that the device is substantially equivalent to a legally marketed predicate device and can be marketed.

    However, the document does not contain any information regarding acceptance criteria, device performance studies, sample sizes, data provenance, expert ground truth establishment, adjudication methods, multi-reader multi-case studies, or standalone algorithm performance. Such detailed technical study results are typically found in the 510(k) submission itself, which is not fully included here, or in associated scientific publications.

    The document only states the "Indications For Use" for the device: "For use by a dental professional for the purpose of cleaning teeth." This indicates the intended purpose of the device, but not its performance metrics or how those metrics were tested.

    Therefore, I cannot fulfill the request to describe the acceptance criteria and the study that proves the device meets the acceptance criteria, as the necessary information is absent from the provided text.

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    K Number
    K972871
    Device Name
    GENESIS
    Date Cleared
    1997-10-02

    (59 days)

    Product Code
    Regulation Number
    872.3660
    Panel
    Dental
    Reference & Predicate Devices
    N/A
    Predicate For
    N/A
    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
    Intended Use

    For use by a dental professional in obtaining a reproduction of teeth and investing tissues, as needed.

    Device Description

    Not Found

    AI/ML Overview

    I am sorry, but the provided text from the FDA document does not contain information on the acceptance criteria, device performance, or study details such as sample sizes, ground truth establishment, or expert qualifications. The document is an FDA 510(k) clearance letter for a dental device called "Genesis Alginato," indicating its substantial equivalence to a legally marketed predicate device for obtaining reproductions of teeth and investing tissues. It outlines regulatory requirements and allows the manufacturer to market the device, but it does not include the technical performance evaluation data you are requesting.

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