Prorhythm
Country not established
- Devices
- 1
What Prorhythm makes
Prorhythm manufactures the Prorhythm Promap Coaxial Mapping Catheter, available in models PRI-MAP-15, PRI-MAP-20, and PRI-MAP-25. These devices are designed for electroanatomical mapping in cardiac electrophysiology procedures, enabling detailed visualization of heart chamber anatomy and electrical activity.
The company’s products fall under FDA Class II device classification and are listed via the 510(k) pathway. The portfolio is regulated under US medical device laws, with devices authorised for commercial distribution in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Prorhythm have in the registry?
The registry currently lists 1 device for Prorhythm. Devices recorded under merged duplicate company entries are counted once.
Which registries list Prorhythm's devices?
Among its 1 most recently registered device, Prorhythm has devices listed in FDA 510(k) (1 device).
What risk classes do Prorhythm's devices fall under?
Among its 1 most recently registered device, the classes recorded for Prorhythm's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Prorhythm in the registry?
The most recently registered devices listed for Prorhythm include PRORHYTHM PROMAP COAXIAL MAPPING CATHETER, MODELS PRI-MAP-15, PRI-MAP-20, PRI-MAP-25.