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illuminator automatic tune vox and interface cable atib
Magna-Lab
Summary: The illuminator automatic tune vox and interface cable atib by Magna-Lab is a Class 2 medical device used for tumor ablation. It is typically used by oncologists and radiologists in clinical settings.
FDA Clearance Information
Pathway
510K
Number
K020993 ↗
Decision Date
May 21, 2002
Product Code
MOS
Device Class
Class 2
Evidence
0 studies
The illuminator automatic tune vox was cleared through the FDA 510(k) pathway on May 21, 2002. It is manufactured by Magna-Lab and classified as a Class 2 device under product code MOS.
What It Is
The illuminator automatic tune vox is a medical device designed for tumor ablation, which involves the destruction of tumor cells using various energy forms. This device likely integrates with imaging systems to precisely target and ablate tumors. It includes an interface cable for connectivity, ensuring seamless integration with other medical equipment.
Clinical Applications
This device is commonly used in oncology and radiology departments for procedures involving tumor ablation. It is particularly useful in minimally invasive settings where precise targeting of tumors is required. Patients with solid tumors, especially those in hard-to-reach areas, may benefit from this technology.
Indications for Use
The FDA has cleared this device for use in tumor ablation procedures. It is intended for patients with tumors that require precise and targeted destruction, often in cases where traditional surgical methods are not feasible.
Practical Considerations
Clinicians should ensure compatibility with existing imaging systems and verify the appropriate settings for different tumor types. The device may come in various sizes to accommodate different clinical needs, and proper training is essential for optimal use.
Frequently Asked Questions
What is the illuminator automatic tune vox used for?
It is used for the ablation of tumors, providing a minimally invasive option for destroying tumor cells.
What specialties typically use this device?
Oncologists and radiologists primarily use this device in clinical settings for tumor ablation procedures.
What are the FDA-cleared indications?
The device is cleared for use in procedures aimed at ablating tumors, particularly in patients where precise targeting is necessary.
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.