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510(k) Data Aggregation

    K Number
    K170454
    Date Cleared
    2017-10-25

    (252 days)

    Product Code
    Regulation Number
    870.1130
    Reference & Predicate Devices
    N/A
    Why did this record match?
    Device Name :

    Automatic Blood Pressure Monitor Model LD-562U, LD-588U & LD-533U

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

    The Scian Automatic Digital Blood Pressure Monitor, Models LD-562U, LD-588U & LD-533U, are devices intended to measure the systolic and diastolic blood pressure and pulse rate of an adult individual by using a non-invasive technique in which an inflatable cuff is wrapped around the upper arm. In addition, they can detect the appearance of irregular heartbeat during measurement, and give a warning signal once the irregular heartbeat is detected.

    Device Description

    Not Found

    AI/ML Overview

    The provided text is a 510(k) summary for a blood pressure monitor. It includes information about the device's intended use and FDA clearance, but it does not contain the detailed study information needed to answer your request about acceptance criteria and study proving device performance.

    Specifically, the document lacks:

    • A table of acceptance criteria and reported device performance.
    • Information about the sample size, data provenance, number of experts, adjudication method, or ground truth used for performance studies.
    • Any mention of a multi-reader multi-case (MRMC) comparative effectiveness study or standalone algorithm performance.
    • Details regarding the training set size or how its ground truth was established.

    This document primarily serves as an FDA clearance letter and an "Indications for Use" statement, not a scientific study report. To get the information you asked for, you would need to consult a different document, such as the actual clinical or performance study report submitted to the FDA, which is not provided here.

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