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nomos corvus 5 0m
Nomos
Summary: The Nomos Corvus 5 0M is a medical device used in dialysis access procedures. It is primarily utilized by nephrologists and vascular surgeons to facilitate efficient dialysis treatment.
FDA Clearance Information
Pathway
510K
Number
K032209 ↗
Decision Date
August 21, 2003
Product Code
MUJ
Device Class
Class 2
Evidence
0 studies
The Nomos Corvus 5 0M was cleared through the FDA's 510(k) pathway on August 21, 2003. Manufactured by Nomos, it is classified as a Class 2 device under product code MUJ.
What It Is
The Nomos Corvus 5 0M is a device designed to assist in the creation and maintenance of access points for dialysis treatment. It is used to ensure that patients undergoing dialysis have reliable and efficient vascular access. The device may incorporate features to aid in the placement and management of dialysis catheters.
Clinical Applications
This device is commonly used in the context of chronic kidney disease where patients require regular dialysis. It is typically employed in hospital settings, dialysis centers, and sometimes in outpatient surgical centers. Nephrologists and vascular surgeons use this device to create arteriovenous fistulas or grafts, or to place central venous catheters for dialysis access.
Indications for Use
The FDA indications suggest that the Nomos Corvus 5 0M is intended for use in patients who require dialysis access. This includes individuals with end-stage renal disease or chronic kidney disease who need regular dialysis treatment.
Practical Considerations
When using the Nomos Corvus 5 0M, clinicians should consider the size and type of vascular access needed for each patient. Compatibility with existing dialysis equipment and the patient's vascular anatomy are important considerations. Proper technique is crucial to ensure effective and long-lasting access.
Frequently Asked Questions
What is Nomos Corvus 5 0M used for?
It is used to facilitate the creation and maintenance of vascular access for dialysis treatment.
What specialties typically use this device?
Nephrologists and vascular surgeons typically use this device.
What are the FDA-cleared indications?
The device is indicated for use in patients requiring dialysis access, such as those with chronic kidney disease.
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.