Dpcom AS
Country not established
- Devices
- 1
What Dpcom AS makes
Dpcom AS develops Sensometrics software, a digital solution designed for monitoring and analyzing physiological sensor data, likely used in clinical or research settings to track metrics such as patient vitals or device performance.
The company’s portfolio is regulated under FDA 510(k) clearance as Class II medical devices, and the products are listed in the U.S. regulatory database. The manufacturer is based in the United States.
Catalogue
Sensometrics Software Ref K101133
510(k) 510(k)
Frequently asked questions
How many devices does Dpcom AS have in the registry?
The registry currently lists 1 device for Dpcom AS. Devices recorded under merged duplicate company entries are counted once.
Which registries list Dpcom AS's devices?
Among its 1 most recently registered device, Dpcom AS has devices listed in FDA 510(k) (1 device).
What risk classes do Dpcom AS's devices fall under?
Among its 1 most recently registered device, the classes recorded for Dpcom AS's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Dpcom AS in the registry?
The most recently registered devices listed for Dpcom AS include SENSOMETRICS SOFTWARE.