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510(k) Data Aggregation

    K Number
    K031835
    Device Name
    HL888RA
    Date Cleared
    2003-07-01

    (29 days)

    Product Code
    Regulation Number
    870.1130
    Reference & Predicate Devices
    N/A
    Predicate For
    N/A
    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
    Intended Use

    Measures automatically human's Systolic, Diastolic blood pressure and heart rate using the oscillometric method. All values can be read out in one LCD Panel .

    The intended for use of this over-the-counter device is for adult patients whose arm circumference between 24-32cm (approx. 8.7" to 12.6" ) .

    Device Description

    H&L Full Automatic (NIBP) Blood Pressure Monitor Trade Name : HL888RA

    AI/ML Overview

    The provided text is a 510(k) premarket notification decision letter from the FDA to Health & Life Corporation, Ltd. for their HL888RA noninvasive blood pressure measurement system. The document confirms that the device is substantially equivalent to legally marketed predicate devices and is approved for market.

    Crucially, the acceptance criteria and the study proving the device meets those criteria are not detailed in this document. This letter is a regulatory approval, not a technical report or study summary. Therefore, I cannot extract the specific information requested about the acceptance criteria or the study from the provided text.

    The document does offer some general information about the device and its intended use:

    • Device Name: H&L Full Automatic (NIBP) Blood Pressure Monitor, Trade Name: HL888RA
    • Regulation Name: Noninvasive blood pressure measurement system
    • Method: Measures Systolic, Diastolic blood pressure and heart rate using the oscillometric method.
    • Intended Use: For adult patients whose arm circumference is between 24-32cm (approx. 8.7" to 12.6").
    • Type of Use: Over-the-counter use.

    To answer your questions, I would need a different type of document, such as a summary of safety and effectiveness data (SSED), a clinical study report, or the 510(k) submission itself which would contain the performance data and acceptance criteria used for substantial equivalence.

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