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union carbide corp computer interface
Union Carbide
Summary: The Union Carbide Corp Computer Interface is a Class 1 medical device used for tumor ablation procedures. It is typically utilized by oncologists and interventional radiologists in clinical settings.
FDA Clearance Information
Pathway
510K
Number
K790336 ↗
Decision Date
April 4, 1979
Product Code
JQP
Device Class
Class 1
Evidence
0 studies
The Union Carbide Corp Computer Interface was cleared through the FDA 510(k) pathway on April 4, 1979. Manufactured by Union Carbide, it is classified as a Class 1 device under product code JQP.
What It Is
The Union Carbide Corp Computer Interface is a medical device designed to assist in tumor ablation procedures. It serves as a computer interface that facilitates the precise targeting and destruction of tumor tissue. The device integrates with existing ablation systems to enhance accuracy and efficiency, making it a valuable tool in oncological interventions.
Clinical Applications
This device is commonly used in oncology and interventional radiology for the ablation of tumors. It is particularly useful in settings where precise targeting of tumor tissue is critical, such as in liver, lung, or kidney tumors. The device is employed in both inpatient and outpatient settings, catering to adult and pediatric populations requiring minimally invasive tumor treatment.
Indications for Use
The FDA indications suggest that this device is intended for use in procedures requiring the ablation of tumor tissues. It is suitable for patients with solid tumors that are accessible for minimally invasive procedures.
Practical Considerations
The Union Carbide Corp Computer Interface is compatible with a range of ablation systems, offering flexibility in clinical use. It is important to ensure proper integration with existing equipment for optimal performance. Clinicians should be trained in its use to maximize its benefits in tumor ablation procedures.
Frequently Asked Questions
What is the Union Carbide Corp Computer Interface used for?
It is used for assisting in tumor ablation procedures, providing a computer interface to enhance precision and efficiency.
What specialties typically use this device?
Oncology and interventional radiology specialties typically use this device in clinical settings.
What are the FDA-cleared indications?
The device is indicated for use in procedures requiring the ablation of tumor tissues, suitable for patients with accessible solid 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.