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uresil subclavian catheter
Uresil
Summary: The Uresil Subclavian Catheter is a medical device used for venous access, typically in patients requiring long-term intravenous therapy. It is primarily used by healthcare professionals in hospital settings.
FDA Clearance Information
Pathway
510K
Number
K863684 ↗
Decision Date
January 6, 1987
Product Code
DQY
Device Class
Class 2
Evidence
0 studies
The Uresil Subclavian Catheter was cleared through the FDA 510k pathway on January 6, 1987. It is manufactured by Uresil and is classified as a Class 2 device under product code DQY.
What It Is
The Uresil Subclavian Catheter is a type of central venous catheter designed for insertion into the subclavian vein. It provides reliable venous access for the administration of medications, fluids, and for blood sampling. The catheter is typically made of biocompatible materials to minimize the risk of thrombosis and infection.
Clinical Applications
This catheter is commonly used in intensive care units, oncology wards, and surgical settings where long-term intravenous access is necessary. It is particularly useful for patients requiring chemotherapy, total parenteral nutrition, or frequent blood draws. The device is often utilized by specialists in critical care, oncology, and surgery.
Indications for Use
The FDA indications for the Uresil Subclavian Catheter include providing venous access for patients who need long-term intravenous therapy. It is suitable for patients with conditions requiring regular medication administration or nutritional support.
Practical Considerations
The Uresil Subclavian Catheter is available in various sizes to accommodate different patient anatomies. It is important to ensure compatibility with other intravenous equipment and to follow sterile technique during insertion to reduce infection risk.
Frequently Asked Questions
What is the Uresil Subclavian Catheter used for?
It is used for providing long-term venous access for the administration of medications, fluids, and for blood sampling.
What specialties typically use this device?
Specialties such as critical care, oncology, and surgery commonly use this device.
What are the FDA-cleared indications?
The device is indicated for providing venous access in patients requiring long-term intravenous therapy.
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.