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510(k) Data Aggregation

    K Number
    K250652
    Device Name
    ECG-AI Low Ejection Fraction (LEF) 12-Lead algorithm (1010)
    Manufacturer
    Date Cleared
    2025-07-28

    (146 days)

    Product Code
    Regulation Number
    870.2380
    Why did this record match?
    Applicant Name (Manufacturer) :

    Anumana, Inc

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdparty
    Intended Use
    The ECG-AI LEF 12-Lead algorithm is software intended to aid in earlier detection of Left Ventricular Ejection Fraction (LVEF) less than or equal to 40% in adults at risk for heart failure. This population includes, but is not limited to: - patients with cardiomyopathies - patients who are post-myocardial infarction - patients with aortic stenosis - patients with chronic atrial fibrillation - patients receiving pharmaceutical therapies that are cardiotoxic, and - postpartum women. The ECG-AI LEF 12-Lead algorithm is not intended to be a stand-alone diagnostic device for cardiac conditions, should not be used for monitoring of patients, and should not be used on ECGs with a paced rhythm. A positive result may suggest the need for further clinical evaluation in order to establish a diagnosis of Left Ventricular Ejection Fraction (LVEF) less than or equal to 40%. Additionally, if the patient is at high risk for the cardiac condition, a negative result should not rule out further non-invasive evaluation. The ECG-AI LEF 12-Lead Algorithm should be applied jointly with clinician judgment.
    Device Description
    The ECG-AI LEF 12-Lead algorithm interprets 12-lead ECG voltage times series data using an artificial intelligence-based algorithm. The device analyzes 10 seconds of a single 12-lead ECG acquisition, and within seconds provides likelihood of LVEF (ejection fraction less than or equal to 40%) to third party software. The results are displayed by the third party software on a device such as a smartphone, tablet, or PC. The ECG-AI LEF 12-Lead algorithm was trained to detect Low LVEF using positive and control cohorts, and the detection of Low LVEF in patients is generated using defined conditions and covariates. The ECG-AI LEF 12-Lead algorithm device is intended to address the unmet need for a point-of-care screen for LVEF less than or equal to 40% and is expected to be used by cardiologists, frontline clinicians at primary care, urgent care, and emergency care settings, where cardiac imaging may not be available or may be difficult or unreliable for clinicians to operate. Clinicians will use the ECG-AI LEF 12-Lead algorithm to aid in earlier detection of LVEF less than or equal to 40% and making a decision for further cardiac evaluation. The software module can be integrated into a client application to be accessed by clinicians and results viewed through an Electronic Medical Record (EMR) system or an ECG Management System (EMS) accessed via a PC, mobile device, or another medical device. In each case, the physician imports 12-lead ECG data in digital format. The tool analyzes the 10 seconds or longer duration of voltage data collected during a standard 12-lead ECG and outputs a binary result of the likelihood of low ejection fraction as an API result.
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    K Number
    K233160
    Device Name
    NeuTrace EP Mapping System v.2.1
    Manufacturer
    Date Cleared
    2023-11-25

    (59 days)

    Product Code
    Regulation Number
    870.1425
    Why did this record match?
    Applicant Name (Manufacturer) :

    Anumana, Inc

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdparty
    Intended Use
    The NeuTrace EP Mapping System v2.1 is indicated for catheter-based cardiac electrophysiological (EP) procedures. The NeuTrace EP Mapping System v2.1 provides information about the electrical activity of the heart and about catheter location during the procedure. The system can be used on patients who are eligible for a conventional electrophysiological procedure in the right atrium. The system has no special contraindications.
    Device Description
    The NeuTrace EP Mapping System v2.1 (NeuTrace System) is an advanced 3D electroanatomical mapping (EAM) and analysis system capable of: - Displaying catheter location during electrophysiology mapping procedures - Displaving 3D images of cardiac structures - Displaying cardiac activity signals as waveforms (ECGs and EGMs) - Displaying derived voltage and time metric overlays over cardiac models -. including Peak-to-Peak Voltage, Local Activation Time (LAT), Fractionation, and Minimum dV/dt The NeuTrace System comprises the following software and hardware components: - NeuTrace Workstation - Window field generator - System control unit - System interface unit - Interface switches and connection cables - NeuTrace Software Application v2.1 - NeuTrace Streaming Application Software v2.0 0 The NeuTrace System is used together with compatible recording systems and compatible catheters listed in the device labeling to perform its intended use to support electrophysiology procedures in the right atrium.
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    K Number
    K232699
    Device Name
    Low Ejection Fraction AI-ECG Algorithm
    Manufacturer
    Date Cleared
    2023-09-28

    (23 days)

    Product Code
    Regulation Number
    870.2380
    Why did this record match?
    Applicant Name (Manufacturer) :

    Anumana, Inc

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdparty
    Intended Use
    The Anumana Low Ejection Fraction AI-ECG Algorithm is software intended to aid in screening for Left Ventricular Ejection Fraction (LVEF) less than or equal to 40% in adults at risk for heart failure. This population includes, but is not limited to: · patients with cardiomyopathies - patients who are post-myocardial infarction - · patients with aortic stenosis - · patients with chronic atrial fibrillation - · patients receiving pharmaceutical therapies that are cardiotoxic, and • postpartum women. Anumana Low Ejection Fraction Al-ECG Algorthm is not intended to be a stand-alone diagnostic device for cardiac conditions, should not be used for monitoring of patients, and should not be used on ECGs with a paced rhythm. A positive result may suggest the need for further clinical evaluation in order to establish a diagnosis of Left Ventricular Ejection Fraction (LVEF) less than or equal to 40%. Additionally, if the patient is at high risk for the cardiac condition, a negative result should not rule out further non-invasive evaluation. The Anumana Low Ejection Fraction AI-ECG Algorithm should be applied jointly with clinician judgment.
    Device Description
    The Low Ejection Fraction AI-ECG Algorithm interprets 12-lead ECG voltage times series data using an artificial intelligence-based algorithm. The device analyzes 10 seconds of a single 12lead ECG acquisition, and within seconds provides a prediction of likelihood of LVEF (ejection fraction less than or equal to 40%) to third party software. The results are displayed by the third-party software on a device such as a smartphone, tablet, or PC. The Low Ejection Fraction AI-ECG Algorithm was trained to predict Low LVEF using positive and control cohorts, and the prediction of Low LVEF in patients is generated using defined conditions and covariates. The Low Ejection Fraction AI-ECG Algorithm device is intended to address the unmet need for a point-of-care screen for LVEF less than or equal to 40% and is expected to be used by cardiologists, front-line clinicians at primary care, urgent care, and emergency care settings, where cardiac imaging may not be available or may be difficult or unreliable for clinicians to operate. Clinicians will use the Low Eiection Fraction AI-ECG Algorithm to aid in screening for LVEF less than or equal to 40% and making a decision for further cardiac evaluation.
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