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rt-200 computer interface
Timeter Instrument
Summary: The rt-200 computer interface by Timeter Instrument is a Class 1 medical device used primarily for tumor ablation procedures. It is typically utilized by oncologists and interventional radiologists.
FDA Clearance Information
Pathway
510K
Number
K875075 ↗
Decision Date
April 21, 1988
Product Code
BXX
Device Class
Class 1
Evidence
0 studies
The rt-200 computer interface was cleared through the FDA 510k pathway on April 21, 1988. Manufactured by Timeter Instrument, it is classified as a Class 1 device under product code BXX.
What It Is
The rt-200 computer interface is a medical device designed to facilitate the ablation of tumors. It works by interfacing with other ablation equipment to provide precise control and monitoring during procedures. This device is essential in ensuring accuracy and safety when targeting tumor tissues, making it a valuable tool in oncological interventions.
Clinical Applications
Commonly used in oncology and interventional radiology, the rt-200 computer interface is integral in procedures requiring tumor ablation. It is used in both hospital and outpatient settings, particularly for patients with tumors that are candidates for minimally invasive ablation techniques. The device supports clinicians in delivering targeted treatment while minimizing damage to surrounding healthy tissues.
Indications for Use
The FDA-cleared indications for the rt-200 computer interface involve its use in tumor ablation procedures. It is intended for patients with tumors that can be treated through ablation, offering a minimally invasive option for tumor management.
Practical Considerations
The rt-200 computer interface is typically compatible with a range of ablation devices, allowing for flexible integration into existing clinical workflows. Clinicians should ensure proper calibration and setup to maximize the device's effectiveness and safety during procedures.
Frequently Asked Questions
What is rt-200 computer interface used for?
The rt-200 computer interface is used for facilitating tumor ablation procedures, providing control and monitoring capabilities.
What specialties typically use this device?
Oncology and interventional radiology specialties typically use this device for tumor ablation procedures.
What are the FDA-cleared indications?
The device is indicated for use in tumor ablation procedures, offering a minimally invasive treatment option for patients with 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.