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510(k) Data Aggregation

    K Number
    K053216
    Date Cleared
    2006-02-10

    (85 days)

    Product Code
    Regulation Number
    874.1050
    Reference & Predicate Devices
    N/A
    Why did this record match?
    Device Name :

    HEARID WIDEBAND MIDDLE EAR POWER ANALYZER

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

    The intended use of the HearID-wbMEPA Middle Ear Power Analyzer is to characterize the middle ear status and to assist in diagnosing middle ear pathologies. The HearID-wbMEPA system measures various acoustic properties of the ear, namely power reflectance, power absorption, transmittance, reflectance group delay, complex acoustic impedance and admittance, and equivalent ear canal volume. These measures allow the evaluation of the functional condition of the middle and outer ear. The devices are suitable for all populations including new-born infants. The devices are to be used by trained personnel only.

    Device Description

    The HearID system comes in two versions: HearID_b-wbMEPA, and HearID_e-wbMEPA, where the difference is the variation of the hardware platform.

    AI/ML Overview

    The provided text is a 510(k) premarket notification approval letter for the HearID Wideband Middle Ear Power Analyzer. It confirms that the device is substantially equivalent to a legally marketed predicate device.

    *However, this document does not contain any information regarding specific acceptance criteria, device performance results, sample sizes for test or training sets, ground truth establishment, expert qualifications, or details about comparative effectiveness studies.

    The letter focuses on regulatory approval based on substantial equivalence, rather than detailing the results of performance studies against predefined acceptance criteria. To provide the requested information, a different document, such as the actual 510(k) submission or a clinical study report, would be necessary.

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