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510(k) Data Aggregation

    K Number
    K991905
    Date Cleared
    1999-09-01

    (89 days)

    Product Code
    Regulation Number
    884.2740
    Reference & Predicate Devices
    Why did this record match?
    Reference Devices :

    K920376, K852608

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

    I. Fetal Surveillance
    The Corometrics® Model 171/172 Series Monitors are used for monitoring of the fetus during the antepartum period as well as throughout labor and delivery (i.e. fetal heart rate and uterine activity monitoring). The device also has an optional monitoring mode to detect fetal body movements.

    II. Maternal NBP Recording
    Blood Pressure. The monitor has an interface to select external NBP monitors. The Monitor does not process any NBP data but only prints the NBP data , from the external monitor, to its chart recorder.

    Device Description

    The Model 171/172 Series Fetal Monitor is intended for monitoring fetal and maternal vital signs: fetal heart rate and maternal uterine activity, fetal movement detection, and an interface for select maternal NIBP monitors. The device is intended for use in a hospital/clinical environment.

    AI/ML Overview

    The provided text is a 510(k) summary for the Corometrics® Model 171/172 Fetal Monitor. It describes the device, its intended use, and comparison to predicate devices. However, it does not contain any information about acceptance criteria, a study proving the device meets acceptance criteria, or any of the specific details requested in your prompt related to the performance study (sample size, data provenance, ground truth, experts, adjudication, MRMC, standalone performance, training set, etc.).

    The document explicitly states:

    • "To date, no performance standards relating to devices of this type have been promulgated by the Food and Drug Administration." This indicates that there are no FDA-mandated performance "acceptance criteria" for this device type.
    • "The Model 171/172 Series Fetal Monitor has been extensively tested to meet its requirements and design." While it mentions "extensively tested," it does not provide details of what those requirements were, the results of the tests, or a study demonstrating performance against specific criteria.

    Therefore, I cannot populate the table or answer the specific questions about a performance study, as the necessary information is not present in the provided text.

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