Topera's FIRMap Catheter Receives 510(k) Clearance

Topera Medical has received 510(k) clearance by the FDA for the FIRMap catheter. The Topera 3D mapping system, which consists of the RhythmView workstation and the FIRMap diagnostic catheter, is designed to improve patient outcomes by enabling electrophysiologists to view a dynamic representation of the electrical activity of the heart, supporting the diagnosis of and treatment planning for a variety of arrhythmias including atrial fibrillation, atrial flutter, atrial tachycardia, and ventricular tachycardia.

This article is tagged to:
Sector: Medical Devices
Geography: United States

Enter your details to read the full article

By submitting this form you are acknowledging that you have read and understood our Privacy Policy.