X-Trodes
IsraelFDA 510(k) applicant, unverified
- Devices
- 1
What X-Trodes makes
X-Trodes manufactures the X-trodes System M, a medical device designed for electrophysiological mapping and ablation procedures in cardiac electrophysiology. This system is intended for use in catheter-based interventions to diagnose and treat arrhythmias by providing detailed mapping of heart chamber electrical activity.
The X-trodes System M is classified as a Class II device under FDA regulations and is authorised via the 510(k) clearance process. The company is based in the United States.
Catalogue
X-trodes System M Ref K232210
510(k) 510(k)
Frequently asked questions
How many devices does X-Trodes have in the registry?
The registry currently lists 1 device for X-Trodes. Devices recorded under merged duplicate company entries are counted once.
Which registries list X-Trodes's devices?
Among its 1 most recently registered device, X-Trodes has devices listed in FDA 510(k) (1 device).
What risk classes do X-Trodes's devices fall under?
Among its 1 most recently registered device, the classes recorded for X-Trodes's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from X-Trodes in the registry?
The most recently registered devices listed for X-Trodes include X-trodes System M.