Rhythmia Medical, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
What Rhythmia Medical, Inc. makes
Rhythmia Medical, Inc. manufactures electroanatomical mapping catheters and systems designed for cardiac electrophysiology procedures. The Rhythmia Mapping Catheter and IntellaMap Orion High Resolution Mapping Catheter enable detailed mapping of heart arrhythmias. The Rhythmia Mapping System integrates with these catheters to provide real-time visualization and analysis of cardiac electrical activity during diagnostic and ablation procedures.
These devices are classified as Class II under FDA regulations and are authorised via the 510(k) clearance process. The company is based in the United States.
Catalogue
Rhythmia Mapping Catheter Ref K122461
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Rhythmia Mapping System Ref K130750
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Rhythmia Medical, Inc. have in the registry?
The registry currently lists 3 devices for Rhythmia Medical, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Rhythmia Medical, Inc.'s devices?
Among its 3 most recently registered devices, Rhythmia Medical, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Rhythmia Medical, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Rhythmia Medical, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Rhythmia Medical, Inc. in the registry?
The most recently registered devices listed for Rhythmia Medical, Inc. include RHYTHMIA MAPPING CATHETER, IntellaMap Orion High Resolution Mapping Catheter and RHYTHMIA MAPPING SYSTEM.