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510(k) Data Aggregation

    K Number
    K191614
    Date Cleared
    2019-12-18

    (183 days)

    Product Code
    Regulation Number
    870.2910
    Reference & Predicate Devices
    N/A
    Predicate For
    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
    Intended Use

    The BioSticker System is a remote monitoring system intended for use by healthcare professionals for continuous collection of physiological data in home and healthcare settings while the patient is at rest. This can include heart rate, respiratory rate, and skin temperature. Data are transmitted via wireless connection from the BioSticker for storage and analysis.

    The device is intended for use on general care patients who are 21 years of age or older as a general patient monitor, to provide physiological information. The BioSticker System are intended for use by healthcare professionals as an aid to diagnosis and treatment.

    The device is not intended to measure physiological parameters while the patient undergoes significant motion or is active. The device is not intended for use on critical care patients.

    Device Description

    The BioSticker System is a remote monitoring system intended for use by healthcare professionals for continuous collection of physiological data in home and healthcare settings while the patient is at rest. This can include heart rate, respiratory rate, and skin temperature. Data are transmitted via wireless connection from the BioSticker for storage and analysis.

    AI/ML Overview

    The provided text is a 510(k) clearance letter from the FDA for the BioSticker System. It primarily details the regulatory approval process and the intended use of the device. The document does not contain information about acceptance criteria, device performance studies, or ground truth establishment.

    Therefore, I cannot fulfill your request to describe the acceptance criteria and the study proving the device meets them based on the provided input. The specific information you asked for (e.g., sample sizes, expert qualifications, adjudication methods, MRMC studies, standalone performance, ground truth types) is not present in this regulatory document.

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