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mod dm-356 ips interface module
Extracorporeal Medical Specialities
Summary: The mod dm-356 ips interface module is a medical device used for tumor ablation. It is primarily utilized by oncologists and interventional radiologists in clinical settings.
FDA Clearance Information
Pathway
510K
Number
K800771 ↗
Decision Date
May 20, 1980
Product Code
FKQ
Device Class
Class 2
Evidence
0 studies
The mod dm-356 ips interface module was cleared through the FDA 510(k) pathway on May 20, 1980. It is manufactured by Extracorporeal Medical Specialities and is classified as a Class 2 device.
What It Is
The mod dm-356 ips interface module is a component used in tumor ablation procedures. It functions by interfacing with other ablation equipment to deliver precise energy to target tissues, effectively destroying tumor cells. This device is crucial for ensuring accurate energy delivery and monitoring during the ablation process.
Clinical Applications
This device is commonly used in oncology and interventional radiology for the ablation of tumors. It is typically employed in hospital settings, particularly in radiology departments or specialized cancer treatment centers. Patients with solid tumors, such as liver or kidney tumors, are often candidates for procedures involving this device.
Indications for Use
The FDA indications suggest that this device is intended for use in procedures that require the ablation of tumors. It is suitable for patients with specific types of tumors that can be targeted and treated with ablation techniques.
Practical Considerations
Clinicians should consider the compatibility of the mod dm-356 ips interface module with existing ablation systems. Proper training in the use of this device is essential to ensure effective and safe tumor ablation procedures.
Frequently Asked Questions
What is mod dm-356 ips interface module used for?
It is used for the ablation of tumors, delivering precise energy to target tissues to destroy tumor cells.
What specialties typically use this device?
Oncologists and interventional radiologists typically use this device in clinical settings.
What are the FDA-cleared indications?
The device is indicated for use in tumor ablation procedures, targeting specific types of tumors for treatment.
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.