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510(k) Data Aggregation

    K Number
    K965063
    Manufacturer
    Date Cleared
    1997-01-27

    (40 days)

    Product Code
    Regulation Number
    874.3300
    Reference & Predicate Devices
    Why did this record match?
    Device Name :

    AUDIOTONE (A-552)

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

    To amplify and transmit sound to the ear.

    Device Description

    BTE Hearing Aid

    AI/ML Overview

    The provided text does not contain information about the acceptance criteria or a study proving that the Audiotone A-552 BTE device meets such criteria. The document is a "Summary of Safety and Effectiveness" which outlines basic device information, classification, intended use, and equivalence to a previously cleared device.

    Therefore, I cannot fulfill the request for tables and descriptions regarding acceptance criteria and study details.

    The provided text does NOT contain the following information:

    1. A table of acceptance criteria and the reported device performance
    2. Sample size used for the test set and the data provenance
    3. Number of experts used to establish the ground truth for the test set and their qualifications
    4. Adjudication method for the test set
    5. If a multi-reader multi-case (MRMC) comparative effectiveness study was done, or its effect size
    6. If a standalone (i.e. algorithm only without human-in-the-loop performance) was done
    7. The type of ground truth used
    8. The sample size for the training set
    9. How the ground truth for the training set was established

    The document states: "Dahlberg utilizes the ANSI S3.22-1987 methodology to test and obtain performance data for hearing aids." While this specifies a standard used for testing, it does not provide the acceptance criteria (i.e., specific thresholds the device must meet to be deemed acceptable) nor the results of a study demonstrating compliance with those criteria.

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