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scoutpro 7f long catheters
Biotronik
Summary: The scoutpro 7f long catheters by Biotronik are used in venous stenting procedures. They are typically utilized by interventional radiologists and cardiologists for vascular access and treatment.
FDA Clearance Information
Pathway
510K
Number
K093303 ↗
Decision Date
November 20, 2009
Product Code
DQY
Device Class
Class 2
Evidence
0 studies
The scoutpro 7f long catheters were cleared through the FDA 510(k) pathway on November 20, 2009. Manufactured by Biotronik, this device is classified as Class 2 under product code DQY.
What It Is
The scoutpro 7f long catheters are medical devices designed for use in venous stenting procedures. These catheters facilitate the delivery of stents to targeted venous sites, ensuring precise placement. They are constructed to navigate the vascular system effectively, providing a conduit for stent deployment.
Clinical Applications
These catheters are commonly used in interventional radiology and cardiology settings. They are employed during procedures that require venous stenting, such as treating venous obstructions or insufficiencies. The device is suitable for use in adult patients who require vascular intervention, particularly in hospital or specialized clinic environments.
Indications for Use
The scoutpro 7f long catheters are indicated for use in procedures that involve the placement of venous stents. They are designed to assist in the treatment of conditions such as venous blockages, ensuring proper blood flow and reducing symptoms associated with venous insufficiency.
Practical Considerations
The scoutpro 7f long catheters are typically compatible with a range of stent sizes, making them versatile for various procedures. Clinicians should ensure proper sizing and compatibility with other procedural equipment. Familiarity with catheter navigation techniques is essential for optimal use.
Frequently Asked Questions
What is scoutpro 7f long catheters used for?
The scoutpro 7f long catheters are used for delivering and placing venous stents in patients with venous obstructions or insufficiencies.
What specialties typically use this device?
Interventional radiologists and cardiologists typically use this device during vascular procedures.
What are the FDA-cleared indications?
The device is indicated for use in procedures involving the placement of venous stents to treat venous blockages and insufficiencies.
Disclaimer: This page compiles publicly available regulatory and published clinical evidence for educational reference.
It does not constitute medical advice, product endorsement, or a recommendation for clinical use.
Always consult manufacturer documentation and clinical judgment for patient care decisions.