Cardiosolutions
Country not established
- Devices
- 5
What Cardiosolutions makes
Cardiosolutions manufactures steerable introducers, specifically the Percu-Pro 65cm and 80cm models.
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
Cardiosolutions Percu-Pro Steerable Introducer Ref K131332
Regimes: 510(k) Registry: 510(k)Percu-Pro Guidewire Ref K094062
Regimes: 510(k) Registry: 510(k)Percupro Messenger Balloon Catheter Ref K094048
Regimes: 510(k) Registry: 510(k)Cardiosolutions Dexterity Steerable Introducer Ref K140015
Regimes: 510(k) Registry: 510(k)Cariosolutions Percu-Pro Steerable Introdcer 65cm Cariosolutions Percu-Pro Steerable Introducer 80cm Ref K120086
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Cardiosolutions have in the registry?
The registry currently lists 5 devices for Cardiosolutions. Devices recorded under merged duplicate company entries are counted once.
Which registries list Cardiosolutions's devices?
Among its 5 most recently registered devices, Cardiosolutions has devices listed in FDA 510(k) (5 devices).
What risk classes do Cardiosolutions's devices fall under?
Among its 5 most recently registered devices, the classes recorded for Cardiosolutions's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Cardiosolutions in the registry?
The most recently registered devices listed for Cardiosolutions include CARDIOSOLUTIONS PERCU-PRO STEERABLE INTRODUCER, PERCU-PRO GUIDEWIRE, PERCUPRO MESSENGER BALLOON CATHETER and CARDIOSOLUTIONS DEXTERITY STEERABLE INTRODUCER.