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daig type o4 vs-1 connector
Daig
Summary: The Daig Type O4 VS-1 Connector is a medical device used in the context of IVC filters. It is typically utilized by interventional radiologists and vascular surgeons for procedures involving venous access.
FDA Clearance Information
Pathway
510K
Number
K863921 ↗
Decision Date
November 24, 1986
Product Code
DTB
Device Class
Class 3
Evidence
0 studies
The Daig Type O4 VS-1 Connector was cleared through the FDA 510k pathway on November 24, 1986. Manufactured by Daig, it is classified as a Class 3 device under product code DTB.
What It Is
The Daig Type O4 VS-1 Connector is a specialized medical device designed to facilitate secure connections in procedures involving inferior vena cava (IVC) filters. It ensures reliable venous access and connectivity, which is crucial for the placement and retrieval of IVC filters. The device is engineered to support the high standards required in vascular interventions.
Clinical Applications
This connector is commonly used in interventional radiology and vascular surgery settings. It plays a critical role in procedures involving the placement of IVC filters, which are used to prevent pulmonary embolism in patients with deep vein thrombosis. The device is particularly relevant in hospitals and specialized vascular centers where such interventions are frequently performed.
Indications for Use
The device is indicated for use in patients requiring the placement of IVC filters, typically those at risk of pulmonary embolism due to deep vein thrombosis. It is suitable for patients who cannot undergo anticoagulation therapy.
Practical Considerations
Clinicians should ensure compatibility with existing IVC filter systems. The connector is designed for ease of use, but proper technique is essential to ensure secure and effective connections. Familiarity with the device's specifications and compatibility is recommended for optimal performance.
Frequently Asked Questions
What is the Daig Type O4 VS-1 Connector used for?
It is used to facilitate secure connections in procedures involving IVC filters, primarily to prevent pulmonary embolism.
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 device is indicated for use in patients requiring IVC filter placement, particularly those at risk of pulmonary embolism and unable to undergo anticoagulation 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.