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510(k) Data Aggregation

    K Number
    K092514
    Date Cleared
    2009-12-04

    (109 days)

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

    UPPERARM DIGITAL BLOOD PRESSURE MONITOR, MODEL: MB-300 SERIES

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

    The model MB-300 Series Upperarm Digital Blood Pressure Monitor is intended for use for the noninvasive measurement of blood pressure (systolic and diastolic) and pulse rate in addrio, in a home use setting. Use may be initiated by the individual or as part of a hypertension monitoring and management program supervise by a health care provider.

    Device Description

    Upperarm Digital Blood Pressure Monitor (Upperarm Digital Sphygmomanometer), Model MB-300 Series

    AI/ML Overview

    The provided text is a letter from the FDA regarding a 510(k) premarket notification for an Upperarm Digital Blood Pressure Monitor. It does not contain the acceptance criteria, reported device performance, or details of a study (like sample size, ground truth, expert information, or specific study types like MRMC or standalone) to prove the device meets said criteria.

    Therefore, I cannot fulfill your request for this information from the provided text. The document confirms that the device is "substantially equivalent" to legally marketed predicate devices, which is the FDA's regulatory decision, but doesn't detail the performance study data itself.

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