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impra dual lumen subclavian catheter
Impra
Summary: The Impra Dual Lumen Subclavian Catheter is a medical device used for venous access, primarily in critical care settings. It is typically used by healthcare professionals such as intensivists and anesthesiologists.
FDA Clearance Information
Pathway
510K
Number
K872163 ↗
Decision Date
October 30, 1987
Product Code
DQY
Device Class
Class 2
Evidence
0 studies
The Impra Dual Lumen Subclavian Catheter was cleared via the FDA 510(k) pathway on October 30, 1987. It is manufactured by Impra and classified as a Class 2 device under product code DQY.
What It Is
The Impra Dual Lumen Subclavian Catheter is a specialized catheter designed for insertion into the subclavian vein. It features dual lumens, allowing for simultaneous administration of medications and fluids, as well as blood sampling. This design is particularly useful in managing patients who require multiple intravenous therapies.
Clinical Applications
This catheter is commonly used in intensive care units and surgical settings for patients needing long-term venous access. It is particularly beneficial for critically ill patients requiring continuous medication infusions, parenteral nutrition, or frequent blood draws. Specialties such as critical care medicine, anesthesiology, and emergency medicine frequently utilize this device.
Indications for Use
The FDA indications for the Impra Dual Lumen Subclavian Catheter include providing venous access for patients who need intravenous therapy. It is suitable for patients requiring simultaneous administration of multiple therapies or frequent blood sampling.
Practical Considerations
The catheter is available in various sizes to accommodate different patient anatomies and clinical needs. It is important to ensure compatibility with other intravenous equipment and to follow aseptic techniques during insertion to minimize infection risk.
Frequently Asked Questions
What is the Impra Dual Lumen Subclavian Catheter used for?
It is used for venous access in patients requiring simultaneous administration of medications and fluids or frequent blood sampling.
What specialties typically use this device?
Specialties such as critical care medicine, anesthesiology, and emergency medicine typically use this device.
What are the FDA-cleared indications?
The device is indicated for providing venous access for patients needing intravenous therapy, particularly for simultaneous administration of multiple therapies or frequent blood sampling.
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.