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dryden scavenger interface system
Dryden
Summary: The Dryden Scavenger Interface System is a medical device used in tumor ablation procedures. It is primarily utilized by oncologists and interventional radiologists to manage tumor removal or reduction.
FDA Clearance Information
Pathway
510K
Number
K842843 ↗
Decision Date
July 27, 1984
Product Code
—
Device Class
—
Evidence
0 studies
The Dryden Scavenger Interface System was cleared through the FDA 510k pathway on July 27, 1984. Manufactured by Dryden, it does not have a specific product code or classification.
What It Is
The Dryden Scavenger Interface System is designed to assist in the safe and effective removal of tumor tissue through ablation. It works by integrating with other ablation devices to capture and manage byproducts of the ablation process, ensuring a cleaner and safer procedure. This system is crucial in maintaining the sterility and efficiency of the operating environment.
Clinical Applications
This device is commonly used in oncology settings, particularly in procedures involving tumor ablation. It is suitable for use in hospitals and specialized cancer treatment centers. The primary users are oncologists and interventional radiologists who perform minimally invasive procedures to treat tumors in various patient populations, including those with liver, lung, or kidney tumors.
Indications for Use
The FDA indications suggest that this device is intended for use in procedures involving the ablation of tumors. It is suitable for patients undergoing treatment for various types of tumors where ablation is considered an appropriate therapeutic option.
Practical Considerations
The Dryden Scavenger Interface System should be compatible with standard ablation equipment. Clinicians should ensure proper integration with existing systems to optimize performance. Familiarity with the device's setup and operation is essential for effective use during procedures.
Frequently Asked Questions
What is the Dryden Scavenger Interface System used for?
It is used in tumor ablation procedures to manage and capture byproducts, ensuring a clean and efficient process.
What specialties typically use this device?
Oncologists and interventional radiologists commonly use this device in tumor ablation procedures.
What are the FDA-cleared indications?
The device is indicated for use in tumor ablation procedures, suitable for patients undergoing treatment for various tumors.
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.