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incare hot ice absorbent interface
Hollister
Summary: The incare hot ice absorbent interface is a medical device used primarily in tumor ablation procedures. It is designed for use by healthcare professionals in oncology and surgical settings.
FDA Clearance Information
Pathway
510K
Number
K913035 ↗
Decision Date
September 25, 1991
Product Code
FRO
Device Class
—
Evidence
0 studies
The incare hot ice absorbent interface was cleared through the FDA 510(k) pathway on September 25, 1991. Manufactured by Hollister, it is classified under product code FRO with no specific class designation.
What It Is
The incare hot ice absorbent interface is a specialized device used in medical procedures involving tumor ablation. It functions as an absorbent barrier, managing fluids and maintaining a controlled environment during the procedure. This device is particularly useful in ensuring precision and safety in ablation techniques.
Clinical Applications
Commonly used in oncology, the incare hot ice absorbent interface is employed during tumor ablation procedures to manage fluid absorption and maintain a sterile field. It is typically utilized in hospital settings by surgical oncologists and interventional radiologists. The device is suitable for adult patients undergoing minimally invasive or open surgical procedures.
Indications for Use
The device is indicated for use in procedures where tumor ablation is performed, helping to manage fluids and maintain a sterile environment. It is suitable for patients undergoing treatment for various types of tumors.
Practical Considerations
The incare hot ice absorbent interface is available in various sizes to accommodate different procedural needs. It is compatible with standard ablation equipment and requires proper placement to ensure effective fluid management. Clinicians should be familiar with its application to maximize its benefits.
Frequently Asked Questions
What is incare hot ice absorbent interface used for?
It is used in tumor ablation procedures to manage fluids and maintain a sterile environment.
What specialties typically use this device?
Oncology and surgical specialties, particularly surgical oncologists and interventional radiologists, use this device.
What are the FDA-cleared indications?
The device is indicated for use in tumor ablation procedures to manage fluids and maintain a controlled environment.
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.