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lifestream centrifugel pump interface 210pi
St. Jude Medical
Summary: The Lifestream Centrifugal Pump Interface 210pi is a medical device used in tumor ablation procedures. It is primarily utilized by interventional radiologists and oncologists in hospital settings.
FDA Clearance Information
Pathway
510K
Number
K933014 ↗
Decision Date
September 28, 1994
Product Code
KFM
Device Class
Class 2
Evidence
0 studies
The Lifestream Centrifugal Pump Interface 210pi was cleared through the FDA 510(k) pathway on September 28, 1994. Manufactured by St. Jude Medical, it is classified as a Class 2 device under product code KFM.
What It Is
The Lifestream Centrifugal Pump Interface 210pi is designed to facilitate the delivery of therapeutic agents during tumor ablation procedures. It operates by providing a controlled flow of fluids, which is crucial for the precision required in ablating tumor tissues. This device is integral in ensuring that the ablation process is both effective and safe, minimizing damage to surrounding healthy tissues.
Clinical Applications
This device is commonly used in interventional oncology, particularly in procedures aimed at treating solid tumors through ablation. It is typically employed in hospital settings where advanced imaging and intervention capabilities are available. Patients with liver, kidney, or lung tumors may benefit from procedures utilizing this device, as it aids in precise delivery of ablation agents.
Indications for Use
The FDA indications suggest that this device is intended for use in procedures that require precise fluid delivery, such as tumor ablation. It is suitable for patients undergoing treatment for solid tumors where targeted ablation is necessary.
Practical Considerations
Clinicians should ensure compatibility with existing ablation systems and verify the appropriate sizing for the specific procedure. Familiarity with the device's interface and operation is essential for optimal performance and patient safety.
Frequently Asked Questions
What is Lifestream Centrifugal Pump Interface 210pi used for?
It is used for delivering therapeutic agents during tumor ablation procedures.
What specialties typically use this device?
Interventional radiologists and oncologists typically use this device.
What are the FDA-cleared indications?
The device is indicated for use in tumor ablation procedures requiring precise fluid delivery.
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.