Livassured BV
NetherlandsFDA applicant, unverified FDA
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA establishment
What Livassured BV makes
Livassured BV manufactures the NightWatch+ US, a device designed for continuous monitoring of respiratory patterns and sleep-related metrics during overnight use.
The NightWatch+ US is classified as a Class II medical device and is listed under FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
NightWatch+ US Ref K243199
Regimes: CE MDR 510(k) Registry: 510(k)
FDA establishments
- Livassured Leiden Zuid-Holland · NL FEI 3017084392
Frequently asked questions
How many devices does Livassured BV have in the registry?
The registry currently lists 1 device for Livassured BV. Devices recorded under merged duplicate company entries are counted once.
Which registries list Livassured BV's devices?
Among its 1 most recently registered device, Livassured BV has devices listed in FDA 510(k) (1 device).
What risk classes do Livassured BV's devices fall under?
Among its 1 most recently registered device, the classes recorded for Livassured BV's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Livassured BV in the registry?
The most recently registered devices listed for Livassured BV include NightWatch+ US.
Which FDA establishments are linked to Livassured BV?
1 FDA establishment is linked to Livassured BV in the registry; they are listed on the company page.