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as 1740 interface module
Narco Scientific
Summary: The AS 1740 Interface Module by Narco Scientific is an FDA-cleared Class 2 device used in tumor ablation procedures. It is primarily utilized by oncologists and interventional radiologists in clinical settings.
FDA Clearance Information
Pathway
510K
Number
K831428 ↗
Decision Date
October 14, 1983
Product Code
DRT
Device Class
Class 2
Evidence
0 studies
The AS 1740 Interface Module was cleared through the FDA 510k pathway on October 14, 1983. Manufactured by Narco Scientific, it is classified as a Class 2 device under product code DRT.
What It Is
The AS 1740 Interface Module is a medical device designed to facilitate tumor ablation procedures. It acts as an interface module that integrates with other ablation equipment to enhance precision and control during the procedure. This device is crucial for ensuring accurate energy delivery to targeted tumor tissues, thereby improving treatment outcomes.
Clinical Applications
This device is commonly used in oncology and interventional radiology for the ablation of tumors. It is particularly useful in minimally invasive procedures where precise targeting of tumor tissues is required. The AS 1740 Interface Module is suitable for use in both outpatient and inpatient settings, catering to a diverse patient population requiring tumor ablation therapy.
Indications for Use
The FDA-cleared indications suggest that the AS 1740 Interface Module is intended for use in procedures involving the ablation of tumors. It is suitable for patients with tumors that are accessible via minimally invasive techniques.
Practical Considerations
The AS 1740 Interface Module is compatible with a range of ablation devices, making it versatile in clinical practice. Clinicians should ensure proper integration with existing equipment to maximize its efficacy. Consideration of the device's compatibility with specific tumor types and locations is essential for optimal outcomes.
Related Literature
The linked study explores the structural dynamics of mitochondrial ATP synthase dimers in Trypanosoma brucei. Key findings include the identification of a dimerization interface critical for structural interactions. Although not directly related to the AS 1740 Interface Module, the study highlights the importance of structural interfaces in biological systems. Limitations include its focus on a specific organism and lack of direct clinical application to tumor ablation.
Frequently Asked Questions
What is AS 1740 Interface Module used for?
The AS 1740 Interface Module is used for facilitating tumor ablation procedures, enhancing precision and control in energy delivery.
What specialties typically use this device?
Oncologists and interventional radiologists typically use this device in clinical settings for tumor ablation.
What are the FDA-cleared indications?
The device is indicated for use in tumor ablation procedures, suitable for patients with tumors accessible via minimally invasive techniques.
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.