Kantron Cardiovascular, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Kantron Cardiovascular, Inc. makes
Kantron Cardiovascular, Inc. manufactures medical devices for cardiac monitoring, including the MONO 2 OXYGEN MONITOR for real-time oxygen saturation tracking and the KANTRON 504 HEARTSTATION for electrocardiogram (ECG) recording and analysis.
These devices are classified as Class II under FDA regulations and are listed via 510(k) clearance. The company operates from the United States.
Catalogue
Mono 2 Oxygen Monitor Ref K812587
Regimes: 510(k) Registry: 510(k)Kantron 504 Heartstation Ref K812586
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Kantron Cardiovascular, Inc. have in the registry?
The registry currently lists 2 devices for Kantron Cardiovascular, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Kantron Cardiovascular, Inc.'s devices?
Among its 2 most recently registered devices, Kantron Cardiovascular, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Kantron Cardiovascular, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Kantron Cardiovascular, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Kantron Cardiovascular, Inc. in the registry?
The most recently registered devices listed for Kantron Cardiovascular, Inc. include MONO 2 OXYGEN MONITOR and KANTRON 504 HEARTSTATION.