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axiom femoral venus catheter
Axiom Medical
Summary: The Axiom Femoral Venous Catheter is a medical device used for venous access in various clinical procedures. It is primarily used by healthcare professionals in hospital settings for patients requiring venous interventions.
FDA Clearance Information
Pathway
510K
Number
K842084 ↗
Decision Date
August 1, 1984
Product Code
DQY
Device Class
Class 2
Evidence
0 studies
The Axiom Femoral Venous Catheter was cleared through the FDA 510k pathway on August 1, 1984. Manufactured by Axiom Medical, it is classified as a Class 2 device under product code DQY.
What It Is
The Axiom Femoral Venous Catheter is a flexible tube designed for insertion into the femoral vein to facilitate venous access. It is used to deliver medications, fluids, or to obtain blood samples. The catheter is typically made of biocompatible materials to minimize the risk of thrombosis and infection.
Clinical Applications
This catheter is commonly used in emergency medicine, critical care, and surgical settings. It is essential for procedures requiring rapid venous access, such as in trauma cases or during major surgeries. The device is suitable for adult patients and can be used in both acute and chronic settings.
Indications for Use
The FDA indications suggest its use for patients needing venous access for therapeutic or diagnostic purposes. This includes patients requiring medication administration, fluid resuscitation, or blood sampling.
Practical Considerations
The catheter is available in various sizes to accommodate different patient anatomies. It is compatible with standard venous access equipment. Clinicians should be trained in proper insertion techniques to minimize complications such as infection or thrombosis.
Frequently Asked Questions
What is the Axiom Femoral Venous Catheter used for?
It is used for venous access to administer medications, fluids, or obtain blood samples.
What specialties typically use this device?
Emergency medicine, critical care, and surgical specialties commonly use this device.
What are the FDA-cleared indications?
The device is indicated for patients needing venous access for therapeutic or diagnostic purposes.
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.