Cardiorhythm
Country not established
- Devices
- 2
What Cardiorhythm makes
Cardiorhythm manufactures diagnostic electrophysiology (EP) catheters, including the VOYAGR and TORQR series, designed for mapping and ablation procedures in cardiac electrophysiology studies.
These devices are classified as Class II under FDA regulations and are authorised through the 510(k) pathway. The company is based in the United States.
Catalogue
Voyagr Series Diagnostic Ep Catheters Ref K923916
Regimes: 510(k) Registry: 510(k)Torqr Series Diagnostic Ep Catheters Ref K923915
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Cardiorhythm have in the registry?
The registry currently lists 2 devices for Cardiorhythm. Devices recorded under merged duplicate company entries are counted once.
Which registries list Cardiorhythm's devices?
Among its 2 most recently registered devices, Cardiorhythm has devices listed in FDA 510(k) (2 devices).
What risk classes do Cardiorhythm's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Cardiorhythm's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Cardiorhythm in the registry?
The most recently registered devices listed for Cardiorhythm include VOYAGR SERIES DIAGNOSTIC EP CATHETERS and TORQR SERIES DIAGNOSTIC EP CATHETERS.