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3m digital disk interface unit
3M
Summary: The 3M Digital Disk Interface Unit is a Class 1 medical device used in tumor ablation procedures. It is primarily utilized by oncologists and interventional radiologists to assist in the precise targeting of tumors.
FDA Clearance Information
Pathway
510K
Number
K920268 ↗
Decision Date
May 27, 1992
Product Code
LMD
Device Class
Class 1
Evidence
0 studies
The 3M Digital Disk Interface Unit was cleared through the FDA 510(k) pathway on May 27, 1992. It is manufactured by 3M and classified as a Class 1 device under product code LMD.
What It Is
The 3M Digital Disk Interface Unit is a medical device designed to facilitate the ablation of tumors. It serves as an interface unit that connects digital imaging systems to ablation devices, allowing for enhanced precision in targeting tumor tissues. This device is particularly useful in procedures where accurate localization of the tumor is critical, thereby improving the efficacy of the ablation process.
Clinical Applications
This device is commonly used in oncology and interventional radiology settings, particularly during procedures that require precise tumor ablation. It is suitable for use in hospitals and specialized cancer treatment centers. The device is typically employed in adult patients with solid tumors that are amenable to ablation, such as liver or kidney tumors.
Indications for Use
The FDA-cleared indications for the 3M Digital Disk Interface Unit involve its use in procedures aimed at ablating tumors. It is intended for patients who require tumor reduction or removal through minimally invasive techniques.
Practical Considerations
Clinicians should ensure compatibility with existing digital imaging systems when using the 3M Digital Disk Interface Unit. Proper training in the use of digital interfaces and ablation techniques is recommended to maximize the device's effectiveness.
Frequently Asked Questions
What is the 3M Digital Disk Interface Unit used for?
It is used to assist in the precise targeting of tumors during ablation procedures.
What specialties typically use this device?
Oncologists and interventional radiologists typically use this device.
What are the FDA-cleared indications?
It is indicated for use in tumor ablation procedures, particularly for targeting 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.