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510(k) Data Aggregation

    K Number
    K100885
    Manufacturer
    Date Cleared
    2010-06-07

    (69 days)

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

    FETAL MONITOR MODEL: BT-200T

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

    The BT-200T is a Fetal Monitor for measuring Fetal Heart Rate, Data is displayed on a front panel LCD display, Fetal heart may be measured by means of Doppler ultrasound.
    BT-200T is pocket size Fetal Monitor for measuring Fetal Heart rate, Pulse Doppler and uterine contraction of pregnant women. It is intended to aid a comprehensive check for the well being of single fetus.

    Device Description

    Bistos' BT-200T is a pocket size Fetal Monitor that measures the fetal heart rate and out puts the fetal sound through built-in speaker. By measuring fetal heart rate (FHR), they are able to predict fetal well-being. BT-200T irradiates ultrasound wave to the abdomen of a pregnant women to detect. The Doppler Frequency signal and analyze, displays the heart rate in LCD screen. The device also provides the heart sound from the heart of fetus.

    AI/ML Overview

    This 510(k) submission for the Bistos BT-200T Fetal Monitor is primarily based on substantial equivalence to a predicate device (Bistos BT-200, K052190). As such, the information provided focuses on demonstrating equivalence rather than detailed de novo efficacy studies with specific acceptance criteria and performance metrics typically found in submissions for novel devices.

    However, Section 9 describes a "Voluntary performed Clinical safety test result attached (E) - *HR Accuracy Measuring Report (E-1)". This is the most relevant section for performance criteria.

    1. Table of Acceptance Criteria and Reported Device Performance

    The provided document refers to an "HR Accuracy Measuring Report (E-1)" but does not present the specific acceptance criteria or the reported performance data within the text. For a full understanding, this report would need to be reviewed.

    Based on the typical requirements for Fetal Heart Rate (FHR) monitors, the acceptance criteria would likely be related to accuracy and precision of FHR measurement compared to a gold standard. Without the actual report, the detailed criteria cannot be specified.

    Hypothetical table (based on common FHR monitor standards and lack of specific data in the document):

    Acceptance Criteria CategorySpecific Metric (Hypothetical)Acceptance Limit (Hypothetical)Reported Device Performance (From E-1 report - Not in provided text)
    FHR AccuracyMean Absolute Difference (MAD)≤ 5 bpmNot specified in provided document
    FHR AccuracyBias (mean difference)≤ 3 bpmNot specified in provided document
    FHR AccuracyStandard Deviation≤ 5 bpmNot specified in provided document
    FHR Detection RangeFHR Detection Range50-240 bpmNot specified in provided document
    False Alarm RateFalse Alarm Rate
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