Cardiopulmonics, Inc.
Country not established
- Devices
- 1
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Central Venous Access Catheter Ref K901701
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Cardiopulmonics, Inc. have in the registry?
The registry currently lists 1 device for Cardiopulmonics, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Cardiopulmonics, Inc.'s devices?
Among its 1 most recently registered device, Cardiopulmonics, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Cardiopulmonics, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Cardiopulmonics, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Cardiopulmonics, Inc. in the registry?
The most recently registered devices listed for Cardiopulmonics, Inc. include CENTRAL VENOUS ACCESS CATHETER.