Search Filters

Search Results

Found 1 results

510(k) Data Aggregation

    K Number
    K131245
    Device Name
    OREGON SCINTIFIC
    Date Cleared
    2014-01-17

    (261 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

    By using oscillometric method, the device measure automatically human's Systolic, Diastolic, mean blood pressure, and heart rate. This device is intended for use on adults for age 18 and above. The cuff size is fit for arm circumference of 22-32 cm. The device has the irregular heartbeat indicator feature. The color bar gives a warning signal with readings. The BPU321 can be compatible with the device of Bluetooth Smart-enabled. All values will be read out in LCD panel.

    Device Description

    Not Found

    AI/ML Overview

    The provided text is a 510(k) premarket notification letter from the FDA regarding the Oregon Scientific BLE Upper Arm Blood Pressure Monitor (BPU 321). It confirms substantial equivalence to a legally marketed predicate device. While it mentions the device measures blood pressure and heart rate using an oscillometric method and is intended for adults aged 18 and above, it does not contain the detailed study information or acceptance criteria for device performance.

    Therefore, I cannot provide the requested table or comprehensive study details. The letter primarily focuses on regulatory approval based on demonstrating substantial equivalence, not on presenting performance study results.

    To fulfill the request, information such as the clinical study protocol, results, and statistical analysis would be required, which are typically found in the full 510(k) submission not included in this document.

    Ask a Question

    Ask a specific question about this device

    Page 1 of 1