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brevet disposable connectors
Brevet
Summary: Brevet Disposable Connectors are used in venous stenting procedures to ensure secure connections. They are primarily used by interventional radiologists and vascular surgeons.
FDA Clearance Information
Pathway
510K
Number
K895753 ↗
Decision Date
November 14, 1989
Product Code
DQY
Device Class
Class 2
Evidence
0 studies
The Brevet Disposable Connectors were cleared through the FDA 510(k) pathway on November 14, 1989. Manufactured by Brevet, this device is classified as Class 2 under product code DQY.
What It Is
Brevet Disposable Connectors are single-use components designed to facilitate secure connections in venous stenting procedures. These connectors help maintain the integrity of the stent placement by ensuring reliable attachment to other procedural components. They are typically made from biocompatible materials to minimize the risk of adverse reactions.
Clinical Applications
These connectors are commonly used in procedures involving the placement of venous stents, particularly in cases of venous obstruction or insufficiency. They are frequently utilized in hospital settings, especially in interventional radiology suites and vascular surgery operating rooms. The primary patient population includes individuals with conditions such as deep vein thrombosis or chronic venous insufficiency.
Indications for Use
The FDA indications suggest these connectors are intended for use in venous stenting procedures. This means they are suitable for patients requiring stent placement to treat conditions like venous blockages or to improve venous blood flow.
Practical Considerations
Brevet Disposable Connectors are available in various sizes to accommodate different stent and catheter dimensions. They are designed to be compatible with standard venous stenting equipment. Clinicians should ensure proper sizing and secure attachment to prevent procedural complications.
Frequently Asked Questions
What is Brevet Disposable Connectors used for?
They are used to secure connections in venous stenting procedures, ensuring the stability of the stent placement.
What specialties typically use this device?
Interventional radiologists and vascular surgeons commonly use this device in their procedures.
What are the FDA-cleared indications?
The connectors are indicated for use in venous stenting procedures, particularly for patients with venous blockages or 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.