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510(k) Data Aggregation

    K Number
    K961593
    Date Cleared
    1996-11-07

    (197 days)

    Product Code
    Regulation Number
    874.3300
    Reference & Predicate Devices
    Predicate For
    N/A
    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
    Intended Use

    The intended use of these models is to amplify sound pressure waves and transmit the signal to the external ear through the medium of air to compensate for impaired hearing.

    Device Description

    Descriptions of the device functions, scientific concepts, and physical and performance characteristics of the above-mentioned Intrastar models are set forth in Attachments 1 and 2.

    AI/ML Overview

    The provided text is a 510(k) summary for a pre-wired faceplate for in-the-ear hearing aids. It describes the device, its intended use, and compares its technical characteristics to two predicate devices. However, this document does not contain information about:

    • Acceptance criteria in the context of a clinical study or performance evaluation.
    • A specific study designed to prove the device meets acceptance criteria.
    • Sample sizes for test sets, data provenance, number of experts, adjudication methods, MRMC studies, standalone performance, or ground truth types, as these are typically associated with studies evaluating diagnostic or AI-driven devices.
    • Training set details.

    The document primarily focuses on establishing substantial equivalence to predicate devices based on technical specifications. Therefore, I cannot extract the requested information.

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