Bartronix
Country not established
- Devices
- 1
What Bartronix makes
Bartronix manufactures the Bartronix In-Bed Activity Monitor, a device designed to track patient movement and activity while in bed, likely for clinical or home monitoring purposes.
The device falls under FDA Class I regulation and is listed via the 510(k) pathway. Bartronix is based in the United States.
Catalogue
Bartronix In-Bed Activity Monitor Ref K914859
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Bartronix have in the registry?
The registry currently lists 1 device for Bartronix. Devices recorded under merged duplicate company entries are counted once.
Which registries list Bartronix's devices?
Among its 1 most recently registered device, Bartronix has devices listed in FDA 510(k) (1 device).
What risk classes do Bartronix's devices fall under?
Among its 1 most recently registered device, the classes recorded for Bartronix's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Bartronix in the registry?
The most recently registered devices listed for Bartronix include BARTRONIX IN-BED ACTIVITY MONITOR.