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510(k) Data Aggregation

    K Number
    K984553
    Date Cleared
    1999-01-14

    (23 days)

    Product Code
    Regulation Number
    880.2910
    Reference & Predicate Devices
    N/A
    Predicate For
    N/A
    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
    Intended Use

    The Talking Digital Thermometer is a non-sterile, reusable clinical thermometer intended for the determination of oral, rectal, and axillary body temperature determination humans

    Device Description

    The Talking Digital Thermometer is a clinical thermometer intended for the determination of oral, rectal, and axillary body temperature determination in humans. In terms of physical requirements and operating parameters, the thermometer conforms to ASTM E1112, "Standard Specification for Electronic Thermometer for Intermittent Determination of Patient Temperature."

    AI/ML Overview

    The provided document for the K-Jump Health Co., Ltd.'s Talking Digital Thermometer (K984553) indicates that the device's conformance to a standard specification acts as its acceptance criteria and basis for substantial equivalence.

    Here's a breakdown of the requested information based only on the provided text:

    1. A table of acceptance criteria and the reported device performance

    Acceptance CriteriaReported Device Performance/Compliance
    Conforms to ASTM E1112, "Standard Specification for Electronic Thermometer for Intermittent Determination of Patient Temperature.""In terms of physical requirements and operating parameters, the thermometer conforms to ASTM E1112, Standard Specification for Electronic Thermometer for Intermittent Determination of Patient Temperature." (Page 0)

    2. Sample sized used for the test set and the data provenance (e.g. country of origin of the data, retrospective or prospective)

    The document does not explicitly state the sample size used for any test set or the data provenance. It only mentions conformance to a standard.

    3. Number of experts used to establish the ground truth for the test set and the qualifications of those experts (e.g. radiologist with 10 years of experience)

    The document does not provide information about experts used to establish ground truth. Conformance to the ASTM standard implies testing conducted according to that standard's methodologies, which would specify measurement devices and procedures, not necessarily human expert consensus for "ground truth" in the way it might be for a diagnostic image.

    4. Adjudication method (e.g. 2+1, 3+1, none) for the test set

    The document does not describe any adjudication method.

    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

    The document does not indicate that a multi-reader multi-case (MRMC) comparative effectiveness study was done. This device is a digital thermometer, not an AI-assisted diagnostic tool.

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

    This refers to the performance of a clinical thermometer. Its performance is inherently "standalone" in that it directly measures and displays temperature. The document states its conformance to ASTM E1112, which implies testing of its accuracy and performance as a standalone device.

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

    For a digital thermometer conforming to ASTM E1112, the "ground truth" would be established by reference temperature standards and calibrated measurement equipment, not expert consensus, pathology, or outcomes data in the typical sense. The standard itself outlines the methods for accuracy verification.

    8. The sample size for the training set

    The document does not mention a training set. This device is a conventional medical device, not a machine learning or AI-based system that would typically have a "training set."

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

    Not applicable, as no training set is mentioned or implied for this type of device.

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