Hospitronic
FranceFDA applicant, unverified
- Devices
- 1
What Hospitronic makes
Hospitronic manufactures sensor-based graphical user interfaces designed for integration with medical devices, enabling user interaction and data visualization in clinical settings.
The company’s products are classified as Class II medical devices under FDA regulations and are listed via the 510(k) pathway. These devices are registered in the United States.
Catalogue
Sensor Gui Ref K923519
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Hospitronic have in the registry?
The registry currently lists 1 device for Hospitronic. Devices recorded under merged duplicate company entries are counted once.
Which registries list Hospitronic's devices?
Among its 1 most recently registered device, Hospitronic has devices listed in FDA 510(k) (1 device).
What risk classes do Hospitronic's devices fall under?
Among its 1 most recently registered device, the classes recorded for Hospitronic's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Hospitronic in the registry?
The most recently registered devices listed for Hospitronic include SENSOR GUI.