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510(k) Data Aggregation

    K Number
    K254085

    Validate with FDA (Live)

    Date Cleared
    2026-01-18

    (31 days)

    Product Code
    Regulation Number
    870.1425
    Age Range
    All
    Reference & Predicate Devices
    Predicate For
    N/A
    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticPediatricDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
    Intended Use

    The intended use of the CARTO™ 3 System is catheter-based cardiac electrophysiological (EP) procedures. The CARTO™ 3 System 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. The system has no special contraindications.

    Device Description

    The CARTO™ 3 EP Navigation System V9.0, is a catheter-based atrial and ventricular mapping system designed to acquire and analyze navigation catheter's location and intracardiac ECG signals and use this information to display 3D anatomical and electroanatomical maps of the human heart. The location information needed to create the cardiac maps and the local electrograms are acquired using specialized mapping catheters and reference devices. The CARTO™ 3 System uses two distinct types of location technology – magnetic sensor technology and Advanced Catheter Location (ACL) technology.

    The CARTO™ 3 System V9.0 consists of the following hardware components:

    • Patient Interface Unit – (PIU Plus or PIU)
    • Workstation with Graphic User Interface (GUI)
    • Wide-Screen monitors, keyboard, and mouse
    • Intracardiac In Port
    • Intracardiac Out Port
    • Power Supply
    • Patches Connection Box and Cables (PU)
    • Pedals
    • Location Pad (LP)
    • Signal Processing Unit (SPU) – supported with PIU only

    All hardware components of the CARTO™ 3 system V9.0 are the same as those found in the predicate device, with improved Patient Interface Unit (PIU Plus).

    AI/ML Overview

    N/A

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