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510(k) Data Aggregation

    K Number
    K013500
    Device Name
    KAVO POLYLUX II
    Manufacturer
    Date Cleared
    2002-01-14

    (84 days)

    Product Code
    Regulation Number
    872.6070
    Panel
    Dental
    Reference & Predicate Devices
    N/A
    Predicate For
    N/A
    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
    Intended Use

    KaVo PolyLUX II is a handpiece for polymerization and is intended exclusively for dental treatment in regular dentistry.

    Device Description

    PolyLUX II is a hand piece with a halogen quartz light source intended for curing dental resins.

    AI/ML Overview

    The provided document K013500 is a 510(k) summary for a dental curing light, PolyLUX II. The summary explicitly states: "Performance Data: None required. The claim of substantial equivalence is based on comparisons of formulations and intended uses of the claimed predicate."

    Therefore, based on the provided text, there is no study conducted to prove the device meets specific acceptance criteria in terms of performance. The regulatory approval was based on demonstrating substantial equivalence to predicate devices, not on a new performance study.

    Given this, I cannot extract the information required in the prompt (acceptance criteria, device performance, sample sizes, expert qualifications, adjudication, MRMC study, standalone performance, ground truth types and establishment methods for training and test sets) because such performance data and studies were explicitly not required and thus not provided in this 510(k) summary.

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