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repair kit quinton triple lumen right atrial cathe
Quinton
Summary: The Repair Kit Quinton Triple Lumen Right Atrial Catheter is a medical device used primarily by clinicians for venous access in cardiac procedures. It is designed for use in hospitals and specialized cardiac care settings.
FDA Clearance Information
Pathway
510K
Number
K853860 ↗
Decision Date
October 18, 1985
Product Code
DQY
Device Class
Class 2
Evidence
0 studies
The device was cleared through the FDA 510(k) pathway on October 18, 1985. Manufactured by Quinton, it is classified as a Class 2 device under product code DQY.
What It Is
The Repair Kit Quinton Triple Lumen Right Atrial Catheter is a specialized catheter designed for insertion into the right atrium via venous access. It features three lumens, allowing for multiple functions such as medication delivery, blood sampling, and hemodynamic monitoring. This device is particularly useful in complex cardiac procedures where reliable venous access is critical.
Clinical Applications
This catheter is commonly used in cardiology and critical care settings for patients requiring central venous access. It is particularly beneficial in procedures involving cardiac monitoring, administration of medications, and fluid management. The device is typically used in hospital settings, particularly in intensive care units and during cardiac surgeries.
Indications for Use
The FDA indications suggest this device is intended for patients needing central venous access for cardiac procedures. It is suitable for conditions requiring precise hemodynamic monitoring and administration of therapeutic agents.
Practical Considerations
The catheter is available in various sizes to accommodate different patient anatomies and clinical needs. Compatibility with standard venous access equipment is expected. Proper insertion technique is crucial to minimize complications such as infection or thrombosis.
Frequently Asked Questions
What is the Repair Kit Quinton Triple Lumen Right Atrial Catheter used for?
It is used for central venous access in cardiac procedures, allowing for medication delivery, blood sampling, and hemodynamic monitoring.
What specialties typically use this device?
Cardiology and critical care specialists commonly use this device in hospital settings, particularly in intensive care units and during cardiac surgeries.
What are the FDA-cleared indications?
The device is indicated for central venous access in patients requiring cardiac monitoring and administration of therapeutic agents.
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.