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510(k) Data Aggregation

    K Number
    K241540
    Device Name
    NUVISION™ Ultrasound Catheter; NUVISION™ NAV Ultrasound Catheter
    Manufacturer
    Biosense Webster, Inc.
    Date Cleared
    2024-06-28

    (28 days)

    Product Code
    OBJ
    Regulation Number
    870.1200
    Why did this record match?
    Applicant Name (Manufacturer) :

    Biosense Webster, Inc.

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
    Intended Use
    The NUVISION™ Ultrasound Catheter is indicated for intracardiac and intra-luminal visualization of cardiac and great vessel anatomy and physiology as well as visualization of other devices in the heart of adult and pediatric patients. The catheter is intended for imaging guidance only, not treatment delivery, during cardiac interventional percutaneous procedures. The NUVISION™ NA V Utrasound Catheter and related accessory devices are indicated for intra-cardiac and intraluminal visualization of cardiac and great vessel anatomy and physiology as well as visualization of other devices in the heart. When used with the compatible CARTO™ 3 EP Navigation System, the catheter provides location information. The catheter is intended for imaging guidance only, not treatment delivery, during cardiac interventional percutaneous procedures.
    Device Description
    The NUVISION™ Catheters are sterile, single use ultrasound catheters. They intended for intra-cardiac and intra-luminal visualization of cardiac and great vessel anatomy and physiology as well as visualization of other devices in the heart of patients. The catheters are intended for imaging guidance only, not treatment or therapy delivery, during cardiac interventional percutaneous procedures. The NUVISION Ultrasound Catheter and NUVISION NAV Ultrasound Catheter are sterile, single-use, disposable intracardiac echo (ICE) ultrasound imaging catheters. The distal end of the catheter has an ultrasound transducer with 2D acoustic element array on ASIC enabling real time 2D, 3D, and multiplane imaging. NUVISION Ultrasound Catheter is compatible with GE Vivid™ S70N and GE E95 Ultrasound System to enable 4D intra-cardiac imaging. While the NUVISION NAV Ultrasound Catheter's grid transducer combines the processing power of the GE Vivid™ S70N Ultrasound System to enable 4D intra-cardiac imaging and when coupled with a 3D location sensor enables location mapping in a compatible CARTO 3 System. The transducer array can be rotated independently of the deflection plane of the catheter shaft. The NUVISION NAV Ultrasound Catheter adds integration into the CARTO environment.
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    K Number
    K240050
    Device Name
    SOUNDSTAR™ CRYSTAL Ultrasound Catheter
    Manufacturer
    Biosense Webster, Inc.
    Date Cleared
    2024-06-12

    (156 days)

    Product Code
    OBJ
    Regulation Number
    870.1200
    Why did this record match?
    Applicant Name (Manufacturer) :

    Biosense Webster, Inc.

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
    Intended Use
    The SOUNDSTAR™ CRYSTAL Ultrasound Catheter and related accessory devices are indicated for intra-cardiac and intra-luminal visualization of cardiac and great vessel anatomy and physiology as well as visualization of other devices in the heart. When used with compatible CARTO™ 3 EP Navigation Systems, the catheter provides location information. Refer to the Compatibility Matrix Insert for compatible CARTO™ 3 Systems as each catheter is compatible with a specific version of the CARTO™ 3 System and is not backward compatible with previous versions of the CARTO™ 3 EP Navigation System.
    Device Description
    The SOUNDSTAR CRYSTAL Ultrasound catheter is disposable and licensed for single use only. The catheter is optimized for intracardiac scanning. With the catheter, the physician can maneuver the imaging plane located inside the catheter tip to see the region of interest. The physician can steer the catheter to optimize tissue visualization. The catheter is to be used only on systems with which they have been tested and found compatible. The proposed device, when connected to the corresponding Ultrasound Systems, will provide real-time integration of ultrasound images with CARTO® 3 EP Navigation System.
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    K Number
    K231207
    Device Name
    CARTO™ 3 EP Navigation System Software V8.0 (FG-5400-00, FG-5400-00U)
    Manufacturer
    Biosense Webster, Inc.
    Date Cleared
    2023-09-07

    (133 days)

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

    Biosense Webster, Inc.

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
    Intended Use
    The intended use of the CARTO™ 3 System is catheter-based cardiac electrophysiological (EP) procedures. The CARTOTM 3 System provides information about the electrical activity of the heart and about catheter location 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 CARTOTM 3 EP Navigation System V8.0, 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 CARTOTM 3 System uses two distinct types of location technology - magnetic sensor technology and Advanced Catheter Location (ACL) technology. The CARTOTM 3 System V8.0 consists of the following hardware components: - Patient Interface Unit (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) All hardware components of the CARTO™ 3 system V8.0 are the same as those found in the predicate device.
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    K Number
    K231412
    Device Name
    CARTO VIZIGO® 8.5F Bi-Directional Guiding Sheath (D-1385-01-S, D-1385-02-S, D-1385-03-S)
    Manufacturer
    Biosense Webster, Inc.
    Date Cleared
    2023-07-10

    (55 days)

    Product Code
    DYB
    Regulation Number
    870.1340
    Why did this record match?
    Applicant Name (Manufacturer) :

    Biosense Webster, Inc.

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
    Intended Use
    The CARTO VIZIGO® 8.5F Bi-Directional Guiding Sheath is indicated for introducing various cardiovascular catheters into the heart, including the left side of the heart through the interatrial septum. The sheath curve can be visualized when used with compatible CARTO® EP Navigation Systems.
    Device Description
    The CARTO VIZIGO® 8.5F Bi-Directional Guiding Sheath is designed to provide accessibility and maneuverability in the cardiac anatomy. The steerable sheath is fitted with a hemostatis valve to minimize blood loss during catheter introduction and/or exchange. A sideport with three-way stopcock is provided for air or blood aspiration, and fluid infusion. A handle equipped with a rotating collar to deflect the tip clockwise ≥ 180° and counterclockwise ≥ 180°. The steerable sheath features distal vent holes to facilitate aspiration and minimize cavitation and a radiopaque tip marker to allow fluoroscopic visualization. The steerable sheath is coated with silicone lubricant on the entire shaft and dilator surface to help minimize friction at the insertion site. The sheath has electrodes on the outer surface to allow interface with compatible CARTO® 3 EP Navigation Systems.
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    K Number
    K230253
    Device Name
    OPTRELL™ Mapping Catheter with TRUEref™ Technology
    Manufacturer
    Biosense Webster, Inc.
    Date Cleared
    2023-03-02

    (30 days)

    Product Code
    MTD
    Regulation Number
    870.1220
    Why did this record match?
    Applicant Name (Manufacturer) :

    Biosense Webster, Inc.

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
    Intended Use
    The OPTRELL™ Mapping Catheter with TRUEref™ Technology is indicated for multiple electrophysiological mapping of cardiac structures in the heart, i.e., recording or simulation only. This catheter is intended to obtain electrograms in the atrial and ventricular regions of the heart. The cather provides location information only when used with a compatible version of the CARTO™ 3 System.
    Device Description
    The OPTRELL™ Mapping Catheter with TRUEref™ Technology has been designed to facilitate electrophysiological mapping of the heart with the CARTO™ 3 System. The OPTRELL™ Mapping Catheter with TRUEref™ Technology is deployed in the heart through an 8.5 F guiding sheath. This bi-directional deflectable catheter includes six (6) parallel 2 Fr spines that are joined to form three (3) loops on the deflectable tip. Each spine has six (6) platinum electrodes that are used for stimulating and recording. The electrodes form a 6 by 6 (6x6) grid. A magnetic location sensor embedded in the deflectable tip transmits location information to the CARTO™ 3 EP Navigation System. Below the spines on the deflectable tip are three (3) electrodes that allow visualization of the tip on the CARTO™ 3 System. The TRUEref™ Electrode, which is embedded in the distal end of the irrigation lumen, can be used as an internal close unipolar reference electrode within the heart chamber. Rotating the catheter's Rocker Lever clockwise or counterclockwise deflects the tip; rotating the Rocker Lever to the neutral position straightens the tip. The catheter includes an irrigation lumen for connection to a source of continuous drip anticoagulant fluid. Lastly, the proposed catheter is offered in the same deflectable curve offerings as the predicate.
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    K Number
    K223733
    Device Name
    CARTO® 3 EP Navigation System with CARTOSOUND™ 4D Version 7.4
    Manufacturer
    Biosense Webster, Inc.
    Date Cleared
    2023-02-16

    (65 days)

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

    Biosense Webster, Inc.

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
    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
    CARTO® The 3 EP Navigation System with CARTOSOUND™ 4D, software V7.4, 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 with CARTOSOUND™ 4D consists of the following hardware components: - . Patient Interface Unit (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) ● All hardware components of the CARTO® 3 system with CARTOSOUND™ 4D are the same to those found in the predicate device.
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    K Number
    K223766
    Device Name
    NUVISION™ NAV Ultrasound Catheter
    Manufacturer
    Biosense Webster, Inc.
    Date Cleared
    2023-02-16

    (63 days)

    Product Code
    OBJ
    Regulation Number
    870.1200
    Why did this record match?
    Applicant Name (Manufacturer) :

    Biosense Webster, Inc.

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
    Intended Use
    The NUVISION™ NA V Ultrasound Catheter and related accessory devices are indicated for intra-cardiac and intraluminal visualization of cardiac and great vessel anatomy and physiology as well as visualization of other devices in the heart. When used with the compatible CARTO™ 3 EP Navigation System, the catheter provides location information. The catheter is intended for imaging guidance only, not treatment delivery, during cardiac interventional percutaneous procedures.
    Device Description
    The NUVISION™ NAV Ultrasound Catheter is a 10F sterile, single-use, disposable diagnostic ultrasound imaging catheter designed for intracardiac use. The distal tip of the catheter contains a 4D ICE ultrasound transducer, comprised of a 2D acoustic element array and ASIC, for real-time 2D, 3D, and multiplane intracardiac imaging. It is coupled with a sensor providing real-time 3D location information to the compatible CARTO™ 3 EP Navigation System with ultrasound capability. Knobs on the catheter handle allow the user to deflect the catheter and rotate the transducer array independently of the deflection of the catheter shaft. The imaging field emanates from one side of the catheter tip, perpendicular to the catheter. The catheter may also be referred to as a probe in some instances.
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    K Number
    K221112
    Device Name
    CARTO 3 EP Navigation System with Advanced Focus Mapping (AFM)
    Manufacturer
    Biosense Webster, Inc.
    Date Cleared
    2022-08-17

    (124 days)

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

    Biosense Webster, Inc.

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
    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 with AFM, software V7.3, is a catheter-based atrial and ventricular mapping system designed to acquire and analyze navigation catheters 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 with AFM consists of the following hardware components: - Patient Interface Unit (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) All hardware components of the CARTO® 3 system with AFM are identical to those described for the predicate device.
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    K Number
    K211438
    Device Name
    OPTRELL Mapping Catheter with TRUEref Technology
    Manufacturer
    Biosense Webster, Inc.
    Date Cleared
    2022-03-18

    (312 days)

    Product Code
    MTD, DRF
    Regulation Number
    870.1220
    Why did this record match?
    Applicant Name (Manufacturer) :

    Biosense Webster, Inc.

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
    Intended Use
    The OPTRELL™ Mapping Catheter with TRUEref™ Technology is indicated for multiple electrophysiological mapping of cardiac structures in the heart, i.e., recording or stimulation only. This catheter is intended to obtain electrograms in the atrial and ventricular regions of the heart. The cather provides location information only when used with a compatible version of the CARTO™ 3 System.
    Device Description
    The OPTRELL™ Mapping Catheter with TRUEref™ Technology is designed to facilitate electrophysiological mapping of the heart with the CARTO™ 3 System. It is designed for deployment in a heart chamber through an 8.5 Fr guiding sheath. This bi-directional deflectable catheter includes six (6) parallel 2 Fr spines that are joined to form three (3) loops on the deflectable tip. Each spine has eight (8) platinum electrodes that are used for stimulating and recording. The electrodes form a 6 by 8 (6x8) grid. A magnetic location sensor embedded in the deflectable tip transmits location information to the CARTO™ 3 EP Navigation System. Below the spines on the deflectable tip are three (3) electrodes that allow visualization of the tip on the CARTO™ 3 System. The TRUEref™ Electrode, which is embedded in the distal end of the irrigation lumen, can be used as an internal close unipolar reference electrode within the heart chamber. Rotating the catheter's Rocker Lever clockwise or counterclockwise deflects the tip; rotating the Rocker Lever to the neutral position straightens the tip. The catheter includes an irrigation lumen for connection to a source of continuous drip anticoagulant fluid.
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    K Number
    K211219
    Device Name
    LASSOSTAR NAV Circular Mapping Catheter
    Manufacturer
    Biosense Webster, Inc.
    Date Cleared
    2022-01-26

    (278 days)

    Product Code
    DRF
    Regulation Number
    870.1220
    Why did this record match?
    Applicant Name (Manufacturer) :

    Biosense Webster, Inc.

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
    Intended Use
    The LASSOSTAR™ NAV Circular Mapping Catheter is indicated for multiple electrode electrophysiology recording and stimulation of the atrial region of the heart. The catheter can be used with a compatible CARTO™ 3 System to provide location information and to create three-dimensional electroanatomic maps. (The catheter is not compatible with CARTO™ 3 Systems prior to Version 7.)
    Device Description
    The Biosense Webster LASSOSTAR™ NAV Circular Mapping Catheter is a 3.5 Fr, multielectrode electrophysiological circular mapping catheter designed to provide location information and to create three-dimensional electroanatomic maps of the heart. On its distal tip, the catheter has a loop with platinum electrodes that can be used for recording and stimulation. The tip has an embedded sensor that allows the catheter to provide location information and create threedimensional electroanatomic maps when used with a compatible Biosense Webster Inc. CARTO™ 3 System. The catheter is available in three loop diameters: 15 mm, 20 mm and 25 mm to allow for use in pulmonary veins of differing size. The catheter can be visualized using conventional systems (such as fluoroscopy or ultrasound imaging), or with a compatible CARTO™ 3 System via interface cables with the appropriate connectors. The LASSOSTAR™ NAV Circular Mapping catheter has three product configurations (D-1404-01-S, D-1404-02-S, D-1404-03-S).
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