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510(k) Data Aggregation

    K Number
    K031978
    Manufacturer
    Date Cleared
    2003-07-21

    (25 days)

    Product Code
    Regulation Number
    874.1090
    Reference & Predicate Devices
    Predicate For
    N/A
    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
    Intended Use

    The Amplaid A756 Screening Admittance Meter can

    • 1 . Evaluate middle ear functions such as otitis media, glue ear, eardrum scar tissues, perform myringotomy status, ossicular chain discontinuity ear canal volume, otosclerosis, stapes fixation.
      1. Perform Acoustic reflex test.
      1. Determine acoustic reflex threshold
      1. Perform reflex decay test.

    The unit is intended for use by a qualified/trained audiologist on both adult and pediatric subjects for measurement of acoustic impedance.

    Device Description

    The Amplaid A756 Screening ADMITTANCE METER performs plane and compensated tympanometry; Programmed and manual stimuli for ipsilateral and contralateral acoustic reflex; Automatic reflex threshold; and Decay measurements.

    AI/ML Overview

    The Amplaid A756 Screening Admittance Meter was determined to be substantially equivalent to the predicate device (Amplaid A724 – A728 ADMITTANCE METERS, K992370) based on bench and user testing. The provided document does not contain explicit acceptance criteria thresholds or detailed study results beyond a general statement of safety and effectiveness.

    Here's the information based on the provided text:

    1. Table of Acceptance Criteria and Reported Device Performance

    The document states that the A756 device is "as safe and effective as the predicate device" after analyzing "bench and user testing data." No specific quantitative acceptance criteria or detailed performance metrics are given in the provided text. The comparison focuses on technical and safety characteristics.

    CharacteristicAcceptance Criteria (Implicit: Equivalence to Predicate)Reported Device Performance (Amplaid A756)
    Intended UseSimilar to predicate: Clinical auditory impedance testing applicationsScreening audiometry impedance testing applications (subset of predicate's use)
    Computer InterfaceRS232 Bi-directionalSAME (RS232 Bi-directional)
    DisplayBuilt-in liquid crystalSAME (Built-in liquid crystal)
    Control InterfaceBuilt-in keyboardSAME (Built-in keyboard)
    Hardcopy OutputBuilt-in Thermal printerSAME (Built-in Thermal printer)
    Audiometric StandardsCompliance with IEC 61027, ANSI S3.39, IEC 60645-1, ANSI S3.6, EN ISO 389SAME (Compliance with listed standards)
    Electrical Safety StandardsCompliance with EN 60601-1 Class I Type BF (1990) and amendments, EMC: EN 60601-1-2 (1993)EN 60601-1 Class I Type B (1990) and amendments, EMC: EN 60601-1-2 (1993) (Note: Type B vs Type BF, but considered substantially equivalent)
    Overall Safety & EffectivenessAs safe and effective as predicate"as safe and effective as the predicate device"

    2. Sample size used for the test set and the data provenance

    The document mentions "bench and user testing" but does not specify the sample size for the test set. It also does not detail the data provenance (e.g., country of origin, retrospective or prospective).

    3. Number of experts used to establish the ground truth for the test set and the qualifications of those experts

    This information is not provided in the document.

    4. Adjudication method for the test set

    This information is not provided in the document.

    5. If a multi reader multi case (MRMC) comparative effectiveness study was done, If so, what was the effect size of how much human readers improve with AI vs without AI assistance

    An MRMC study was not conducted as this device is an Auditory Impedance Tester, not an AI-powered diagnostic tool. The comparison is between two medical devices, not AI assistance for human readers.

    6. If a standalone (i.e. algorithm only without human-in-the-loop performance) was done

    The device is an Auditory Impedance Tester, which is a physical medical device and not an algorithm or AI system. Therefore, a "standalone algorithm-only" performance study is not applicable. The device's performance is inherently standalone in its function, but results are interpreted by a "qualified/trained audiologist."

    7. The type of ground truth used (expert consensus, pathology, outcomes data, etc.)

    The document does not specify the type of ground truth used for validating the "user testing" or "bench testing." It can be inferred that for an auditory impedance tester, validation would typically involve comparing measurements against established audiometric standards or clinical diagnoses, but this is not explicitly stated.

    8. The sample size for the training set

    This information is not applicable as the device is not an AI/machine learning model that typically requires a training set.

    9. How the ground truth for the training set was established

    This information is not applicable as the device is not an AI/machine learning model.

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