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510(k) Data Aggregation

    K Number
    K031695
    Device Name
    HL168R
    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 age 16 and above.

    Device Description

    Full Automatic (NIBP) Blood Pressure Monitor

    AI/ML Overview

    Here's an analysis of the provided text regarding acceptance criteria and device performance:

    No specific acceptance criteria or study details are provided in the given document.

    The document is a 510(k) clearance letter from the FDA for the device "HL168R" (a Full Automatic (NIBP) Blood Pressure Monitor). This letter grants clearance for the device based on a finding of "substantial equivalence" to a legally marketed predicate device.

    The FDA's decision of substantial equivalence often relies on performance data submitted by the manufacturer, but this specific letter does not contain those data or the acceptance criteria used. It refers to the manufacturer's 510(k) premarket notification as the source of the information that led to the determination.

    Therefore, I cannot fulfill the request for a table of acceptance criteria, study details, and specific performance metrics based solely on the provided text.

    To answer your request, I would need access to the actual 510(k) submission document for K031695, not just the FDA clearance letter. That document would contain the detailed studies conducted, their methodologies, and the acceptance criteria applied.

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