Cardiovention, Inc.
United StatesFDA applicant, unverified
- Devices
- 4
What Cardiovention, Inc. makes
Cardiovention, Inc. manufactures systems for cardiac electrophysiology procedures, including the CORX IOS-200 System for intracardiac ultrasound-guided interventions and the CORX System for catheter ablation. The company also produces the PowerBase Console, a modular power and control unit for these procedures, along with modifications to enhance functionality.
The company’s devices are classified as Class II under FDA regulations and are listed in the 510(k) clearance registry. These products are intended for use in the United States, where the manufacturer is based.
Catalogue
Cardiovention Corx Ios-200 System, Model Ios-200 Ref K032068
Regimes: 510(k) Registry: 510(k)Cardiovention Corx System, Model Fg 0001 Ref K012325
Regimes: 510(k) Registry: 510(k)Cardiovention Powerbase Console, Model Pbc-100 Ref K021694
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Cardiovention, Inc. have in the registry?
The registry currently lists 4 devices for Cardiovention, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Cardiovention, Inc.'s devices?
Among its 4 most recently registered devices, Cardiovention, Inc. has devices listed in FDA 510(k) (4 devices).
What risk classes do Cardiovention, Inc.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Cardiovention, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Cardiovention, Inc. in the registry?
The most recently registered devices listed for Cardiovention, Inc. include CARDIOVENTION CORX IOS-200 SYSTEM, MODEL IOS-200, CARDIOVENTION CORX SYSTEM, MODEL FG 0001, CARDIOVENTION POWERBASE CONSOLE, MODEL PBC-100 and MODIFICATION TO CARDIOVENTION POWERBASE CONSOLE, MODEL PCB-100.