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510(k) Data Aggregation

    K Number
    K140862
    Date Cleared
    2014-08-27

    (146 days)

    Product Code
    Regulation Number
    884.2720
    Reference & Predicate Devices
    Why did this record match?
    Reference Devices :

    K101801, K112390, K112163, K041026

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

    The Monica Novii Pod is an intrapartum maternal-fetal monitor that non-invasively measures and displays fetal heart rate (FHR), uterine activity (UA) and maternal heart rate (MHR). The Novii Pod acquires and displays the FHR tracing from abdominal surface electrodes that pick up the fetal ECG (fECG) signal. Using the same surface electrodes, the Pod also acquires and displays the UA tracing from the uterine electromyography (EMG) signal and the MHR tracing from the maternal ECG signal (mECG). The Pod is indicated for use on women who are at >36 completed weeks, in labor, with singleton pregnancies, using surface electrodes on the maternal abdomen.

    The Novii Patch is an accessory to the Novii Pod that connects directly to the Novii Pod and contains the surface electrodes that attach to the abdomen.

    The Novii Interface is an accessory to the Novii Pod which provides a means of interfacing the wireless output of the Novii Pod to the transducer inputs of a CTG Fetal monitor. The Novii Interface enables signals collected by the Novii Pod to be printed and displayed on a CTG Fetal Monitor and sent on to a central network, if connected.

    The Novii Pod maternal-fetal monitor and its accessories are intended for use by healthcare professionals in a clinical setting

    Device Description

    The Monica Novii Pod Fetal-Maternal Monitor is designed as an ambulatory device for the monitoring of a pregnant mother. The monitor enables the abdominal electrophysiological signal to be picked up from three different positions on the maternal abdomen using the 5 electrodes on the Monica Novii Patch. The monitor filters the abdominal signals, converts the abdominal electrophysiological data into a digital format and then processes it in real time to extract the fetal heart rate, maternal heart rate and uterine activity. The result of the processing is transmitted via the Bluetooth connection to the Monica Novii CTG Interface device that is a Monica Approved accessory to the Monica Novii Pod.

    AI/ML Overview

    Here's a breakdown of the acceptance criteria and the studies that prove the Monica Novii Wireless Patch System meets them, based on the provided text:

    1. Table of Acceptance Criteria and Reported Device Performance

    The document provides acceptance criteria for non-clinical tests (Data Transfer Validation and Data Extraction Validation).

    Acceptance Criteria CategorySpecific MetricAcceptance CriteriaReported Device Performance
    Non-Clinical Testing
    Data Transfer ValidationBias difference for Fetal Heart Rate (FHR)Less than 1 BPMDemonstrated compliance (implies bias difference was
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