Cardiovascular Devices, Inc.
United StatesFDA applicant, unverified
- Devices
- 8
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Cdi(R) 2000 Blood Gas Monitor Ref K884228
Regimes: 510(k) Registry: 510(k)Gast Stat Monitoring System Ref K840749
Regimes: 510(k) Registry: 510(k)Cdi(Tm) Extracorporeal Blood Gas System 300 Ref K871221
Regimes: 510(k) Registry: 510(k)The Cdi(R) System 400 Ref K890113
Regimes: 510(k) Registry: 510(k)Modified Gas-Stat(Tm) Monitoring System Ref K864703
Regimes: 510(k) Registry: 510(k)Extracorporeal Blood Gas System Ref K822000
Regimes: 510(k) Registry: 510(k)Intravascular Blood Gas System Ref K843912
Regimes: 510(k) Registry: 510(k)Gas-Stat Monitoring System Ref K831225
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Cardiovascular Devices, Inc. have in the registry?
The registry currently lists 8 devices for Cardiovascular Devices, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Cardiovascular Devices, Inc.'s devices?
Among its 8 most recently registered devices, Cardiovascular Devices, Inc. has devices listed in FDA 510(k) (8 devices).
What risk classes do Cardiovascular Devices, Inc.'s devices fall under?
Among its 8 most recently registered devices, the classes recorded for Cardiovascular Devices, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Cardiovascular Devices, Inc. in the registry?
The most recently registered devices listed for Cardiovascular Devices, Inc. include CDI(R) 2000 BLOOD GAS MONITOR, GAST STAT MONITORING SYSTEM, CDI(TM) EXTRACORPOREAL BLOOD GAS SYSTEM 300 and THE CDI(R) SYSTEM 400.