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510(k) Data Aggregation

    K Number
    K021817
    Date Cleared
    2002-07-11

    (38 days)

    Product Code
    Regulation Number
    878.4400
    Reference & Predicate Devices
    Why did this record match?
    Device Name :

    AARON A950 HIGH FREQUENCY ELECTROSURGICAL GENERATOR, AARON A950 ELECTROSURGICAL GENERATOR, 240V

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

    The Aaron 950 High Frequency Electrosurgical Generator models are intended to be used for all electrosurgical cut, blend, coagulation, fulguration, and bipolar procedures.

    Device Description

    The Aaron 950 High Frequency Electrosurgical Generator is a non-sterile, reusable electrosurgical generator, which is designed to generate high frequencies (RF) of high voltage and low amperage current.

    AI/ML Overview

    The provided text is a 510(k) Safety and Effectiveness Summary for an electrosurgical generator. It declares substantial equivalence to predicate devices and does not describe a study involving algorithms, AI, or performance metrics in a way that would require the specific acceptance criteria and study details requested in the prompt. The summary focuses on regulatory compliance through substantial equivalence, rather than a detailed performance study with specific quantitative acceptance criteria or a human-in-the-loop evaluation for an AI device.

    Therefore, I cannot extract the requested information because the document does not contain it. The information requested (acceptance criteria, sample sizes, ground truth establishment, MRMC studies, standalone performance for AI, etc.) is typically found in the context of performance studies for AI/ML-driven devices, not in a 510(k) summary for a traditional electrosurgical generator establishing substantial equivalence.

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