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510(k) Data Aggregation

    K Number
    K241562
    Device Name
    OutFlo Aortic Valve Dilatation Balloon Catheter
    Manufacturer
    DISA Medinotec
    Date Cleared
    2025-03-11

    (284 days)

    Product Code
    OZT
    Regulation Number
    870.1255
    Why did this record match?
    Product Code :

    OZT

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
    Intended Use
    The OutFlo Aortic Valve Dilatation Balloon Catheter is indicated for balloon aortic valvuloplasty.
    Device Description
    The OutFlo Aortic Valve Dilatation Balloon Catheter (marketing name: OutFlo) is a sterile, single use, Over-the-Wire (OTW) dual-lumen catheter with a hub at the proximal end and a balloon cluster at the distal end. The proposed device consists of a series of parallel balloons on a catheter which, when deployed, provides an outward radial force while also creating an inter balloon space or passage for blood flow. Thus, buildup of pressure in the ventricle is avoided. The dilation catheter is intended to be used in conjunction with a 14F or larger guiding catheter and a 0.035" or smaller guidewire, and Y-connectors, none of which are supplied by the manufacturer. The OutFlo Aortic Valve Dilatation Balloon Catheter is provided in five models. The only difference between the models are the balloon diameter.
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    K Number
    K240967
    Device Name
    ValvuloPro Valvuloplasty Balloon Catheter
    Manufacturer
    Dongguan TT Medical, Inc.
    Date Cleared
    2024-07-31

    (113 days)

    Product Code
    OZT
    Regulation Number
    870.1255
    Why did this record match?
    Product Code :

    OZT

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
    Intended Use
    Device Description
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    K Number
    K231814
    Device Name
    ValvuloPro Valvuloplasty Balloon Catheter
    Manufacturer
    Dongguan TT Medical, Inc
    Date Cleared
    2023-10-12

    (113 days)

    Product Code
    OZT
    Regulation Number
    870.1255
    Why did this record match?
    Product Code :

    OZT

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
    Intended Use
    The ValvuloPro® Valvuloplasty Balloon Catheter is indicated for balloon aortic valvuloplasty.
    Device Description
    The ValvuloPro® Valvuloplasty Balloon Catheters are indicated for balvoon aortic valvuloplasty. It consists of an inflatable balloon on a catheter shaft with multiple lumens for inflation. The effective length of the catheter is 130cm. The y-connector consists of a balloon inflation port and a guidewire lumen. Two radiopaque tantalum marker bands are positioned within the balloon shoulders to provide visual reference points fluoroscopically for balloon positioning within the stricture. The balloon catheter is supplied sterilized by ethylene oxide (EO) for single use.
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    K Number
    K220881
    Device Name
    INOUE BALLOON A
    Manufacturer
    Toray Industries, Inc.
    Date Cleared
    2022-12-18

    (268 days)

    Product Code
    OZT
    Regulation Number
    870.1255
    Why did this record match?
    Product Code :

    OZT

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
    Intended Use
    INOUE BALLOON™ A is intended for balloon aortic valvuloplasty (BAV) in patients with aortic stenosis.
    Device Description
    INOUE BALLOON™ A is intended for the treatment of patients with aortic valvuloplasty (BAV). The device is transported over a guidewire as it is inserted through a percutaneous entry site and expanded with a predetermined amount of the diluted contrast medium by use of specified syringe with extension tube connected to the balloon inflation luer-lock hub. This results in the staged inflation of the balloon from hour-glass to barrel shape. The balloon is stretched and made thinner by pushing the inner tube in during passing thorough the introducer sheath. A radiopaque marker is provided for fluoroscopic positioning of the device across the valve.
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    K Number
    K172932
    Device Name
    True Flow Valvuloplasty Perfusion Catheter
    Manufacturer
    C. R. Bard, Inc.
    Date Cleared
    2017-12-13

    (78 days)

    Product Code
    OZT
    Regulation Number
    870.1255
    Why did this record match?
    Product Code :

    OZT

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
    Intended Use
    The True® Flow Valvuloplasty Perfusion Catheter is indicated for balloon aortic valvuloplasty.
    Device Description
    The True® Flow Valvuloplasty Perfusion Catheter is an over-the-wire co-axial catheter with a balloon fixed at the tip. The balloon enables continuous hemodynamic flow through its central orifice. The catheter is 110 cm long and has two lumen is used to inflate and deflate the balloon and the other permits the use of a guidewire to position the catheter. The balloon inflation luer-lock hub (angled) connects to a syringe inflation device to deliver radiopaque contrast media for inflation. The guidewire luer-lock hub (straight) connects to the guidewire lumen. The balloon is non-compliant and is designed to reach a known diameter and length when inflated within the specified pressure range. Two radiopaque markers are located on the guidewire lumen. These bands are positioned at the proximal and distal balloon shoulders. These markers are provided for fluoroscopic positioning of the device across the aortic valve. Balloon catheter dimensions, nominal pressure, maximum inflation pressure, recommended introducer size, and maximum guidewire size are indicated on the package label.
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    K Number
    K152613
    Device Name
    True Flow Valvuloplasty Perfusion Catheter
    Manufacturer
    C. R. BARD, INC.
    Date Cleared
    2016-01-19

    (127 days)

    Product Code
    OZT
    Regulation Number
    870.1255
    Why did this record match?
    Product Code :

    OZT

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
    Intended Use
    The True™ Flow Valvuloplasty Perfusion Catheter is indicated for balloon aortic valvuloplasty.
    Device Description
    The True™ Flow Valvuloplasty Perfusion Catheter is an over-the-wire co-axial catheter with a balloon fixed at the tip. The balloon enables continuous hemodynamic flow through its central orifice. The catheter is 110 cm long and has two lumens: one lumen is used to inflate and deflate the balloon and the other permits the use of a guidewire to position the catheter. The balloon inflation luer-lock hub (angled) connects to a syringe inflation device to deliver radiopaque contrast media for inflation. The guidewire luerlock hub (straight) connects to the guidewire lumen. The balloon is non-compliant and is designed to reach a known diameter and length when inflated within the specified pressure range. Two radiopaque markers are located on the guidewire lumen. These bands are positioned at the proximal and distal balloon shoulders. These markers are provided for fluoroscopic positioning of the device across the aortic valve. Balloon catheter dimensions, nominal pressure, maximum inflation pressure, recommended introducer size, and maximum quidewire size are indicated on the package label.
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    K Number
    K152150
    Device Name
    V8 Balloon Aortic Valvuloplasty Catheter
    Manufacturer
    InterValve, Inc.
    Date Cleared
    2015-12-18

    (137 days)

    Product Code
    OZT
    Regulation Number
    870.1255
    Why did this record match?
    Product Code :

    OZT

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
    Intended Use
    The V8 Balloon Aortic Valvuloplasty Catheter is indicated for Balloon Aortic Valvuloplasty.
    Device Description
    The V8 Balloon Aortic Valvuloplasty Catheter features an hour glass shaped dilatation balloon on the distal end of a catheter. The catheter is inserted through a percutaneous entry site into the common femoral artery via an introducer sheath and advanced retrograde to the aortic valve. The catheter is always delivered over a guidewire. The balloon is then inflated to dilate the stenotic aortic valve leaflets in an effort to increase valve opening dimensions and systemic blood flow by improving leaflet mobility. The hour glass shaped balloon with the undersized waist segment is intended to minimize over-dilatation of the valve annulus while allowing the full dilation of the valve leaflet. The bulbous proximal balloon segment is appropriately sized for the patient's aortic root dimensions to maximize valve leaflet opening. The V8 Balloon Aortic Valvuloplasty Catheter can be used as both a pre-dilatation and postdilatation device for self-expanding transcatheter heart valves.
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    K Number
    K150667
    Device Name
    True Dilatation Balloon Valvuloplasty Catheter
    Manufacturer
    C.R. Bard, Inc.
    Date Cleared
    2015-06-17

    (93 days)

    Product Code
    OZT
    Regulation Number
    870.1255
    Why did this record match?
    Product Code :

    OZT

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
    Intended Use
    The TrueTM Dilatation Balloon Valvuloplasty Catheter is indicated for balloon aortic valvuloplasty.
    Device Description
    The True™ Dilatation Balloon Valvuloplasty Catheter is an over-the-wire co-axial catheter with a balloon fixed at the tip. The catheter is 110 cm long and has two lumens: one lumen is used to inflate and deflate the balloon and the other permits the use of a guidewire to position the catheter. The balloon inflation luer-lock hub (angled) connects to a syringe inflation device to deliver radiopaque contrast media for inflation. The guidewire luer-lock hub (straight) connects to the guidewire lumen. The balloon is noncompliant and is designed to reach a known diameter and length when inflated within the specified pressure range. Two radiopaque marker bands are provided for fluoroscopic positioning of the device across the aortic valve. These bands are positioned at the proximal and distal balloon shoulders. Balloon catheter dimensions, balloon nominal pressure, maximum inflation pressure, recommended introducer size, and recommended guidewire size are indicated on the package label.
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    K Number
    K142083
    Device Name
    TRUE FLOW VALVULOPLASTY PERFUSION CATHETER
    Manufacturer
    C.R. BARD, INC.
    Date Cleared
    2015-04-17

    (260 days)

    Product Code
    OZT
    Regulation Number
    870.1255
    Why did this record match?
    Product Code :

    OZT

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
    Intended Use
    The True™ Flow Valvuloplasty Perfusion Catheter is indicated for balloon aortic valvuloplasty.
    Device Description
    The True™ Flow Valvuloplasty Perfusion Catheter is an over-the-wire co-axial catheter with a balloon fixed at the tip. The balloon enables hemodynamic flow through its central orifice. The catheter is 110 cm long and has two lumens: one lumen is used to inflate and deflate the balloon and the other permits the use of a guidewire to position the catheter. The balloon inflation luer-lock hub (angled) connects to a syringe inflation device to deliver radiopaque contrast media for inflation. The quidewire luer-lock hub (straight) connects to the guidewire lumen. The balloon is non-compliant and is designed to reach a known diameter and length when inflated within the specified pressure range. Three radiopaque markers are embedded in the balloon wall. These bands are positioned at the proximal and distal balloon shoulders, and in the middle. These bands are provided for fluoroscopic positioning of the device across the aortic valve. Balloon catheter dimensions, nominal pressure, maximum inflation pressure, recommended introducer size, and maximum guidewire size are indicated on the package label.
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    K Number
    K150343
    Device Name
    V8 Transluminal BAV Catheter
    Manufacturer
    InterValve, Inc.
    Date Cleared
    2015-04-03

    (51 days)

    Product Code
    OZT
    Regulation Number
    870.1255
    Why did this record match?
    Product Code :

    OZT

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
    Intended Use
    The V8 Transluminal BAV Catheter is indicated for Balloon Aortic Valvuloplasty.
    Device Description
    The V8 Transluminal BAV Catheter System features an hour glass shaped dilatation balloon on the distal end of a catheter. The catheter is inserted through a percutaneous entry site into the common femoral artery via an introducer sheath and advanced retrograde to the aortic valve. The catheter is always delivered over a guidewire. The balloon is then inflated to dilate the stenotic aortic valve leaflets in an effort to increase valve opening dimensions and systemic blood flow by improving leaflet mobility. The hour glass shaped balloon, with the undersized waist segment, is intended to minimize over-dilatation of the valve annulus while allowing the full dilation of the valve leaflet. The bulbous proximal balloon segment is appropriately sized for the patient's aortic root dimensions to maximize valve leaflet opening.
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