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510(k) Data Aggregation

    K Number
    K030222
    Device Name
    NX SYSTEM
    Date Cleared
    2003-08-19

    (209 days)

    Product Code
    Regulation Number
    870.2910
    Reference & Predicate Devices
    N/A
    Why did this record match?
    Device Name :

    NX SYSTEM

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

    The NX System is intended to be used as a monitoring device when time-critical care is not required. The peripheral devices compatible with the NX System are blood pressure, pulse, weight, oxygen saturation, glucose and PT/INR. The NX System enables the home-bound patient to retrieve data taken by the peripheral devices and forward them to an off-site central location for access by a health care professional.

    Device Description

    The NX System is a Telemedicine Communications Module. It uses a custom PC platform for its patient station (NX Monitoring Station) and has more interface options to stand-alone medical device peripherals. The NX system uses wireless technology to connect to the stand-alone medical devices. It obtains readings from medical device peripherals and forwards those data to the system's Server. The NX System has no internal medical devices.

    AI/ML Overview

    The provided text does not contain information about acceptance criteria or a study proving the device meets acceptance criteria. The document is a 510(k) summary for the American TeleCare NX System, detailing its intended use, classification, predicate devices, and a substantial equivalence determination by the FDA.

    Therefore, I cannot provide the requested information in a table or describe a study based on this document. The document focuses on demonstrating substantial equivalence to a predicate device, not on presenting performance data against specific acceptance criteria for a new study.

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