Arrhythmia Technologies, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Arrhythmia Technologies, Inc. makes
Arrhythmia Technologies, Inc. makes diagnostic electrophysiology catheters, including the Voyagr series of deflectable diagnostic EP catheters.
These devices are classified as Class II medical devices and are listed in the FDA 510(k) registry. The company is based in the United States.
Catalogue
Diagnostic Ep Catheter Ref K915563
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Arrhythmia Technologies, Inc. have in the registry?
The registry currently lists 2 devices for Arrhythmia Technologies, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Arrhythmia Technologies, Inc.'s devices?
Among its 2 most recently registered devices, Arrhythmia Technologies, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Arrhythmia Technologies, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Arrhythmia Technologies, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Arrhythmia Technologies, Inc. in the registry?
The most recently registered devices listed for Arrhythmia Technologies, Inc. include DIAGNOSTIC EP CATHETER and VOYAGR SERIES OF DEFLECTABLE DIAGOSTIC EP CATHETER.