Fimreite Software AS
NorwayFDA applicant, unverified
- Devices
- 1
What Fimreite Software AS makes
Fimreite Software AS produces software-based medical devices for remote patient monitoring and data connectivity, including platforms for transmitting and managing clinical data from implanted cardiac devices. The portfolio includes tools for patient communication, travel alerts, and web-based interfaces to facilitate remote monitoring and coordination with healthcare providers.
The company’s devices are classified as Class II under FDA regulations and are authorised through the 510(k) clearance process. These products are listed in the FDA’s 510(k) database. The manufacturer is based in the United States.
Catalogue
Pacentric Connect, Traveler And Web Ref K100837
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Fimreite Software AS have in the registry?
The registry currently lists 1 device for Fimreite Software AS. Devices recorded under merged duplicate company entries are counted once.
Which registries list Fimreite Software AS's devices?
Among its 1 most recently registered device, Fimreite Software AS has devices listed in FDA 510(k) (1 device).
What risk classes do Fimreite Software AS's devices fall under?
Among its 1 most recently registered device, the classes recorded for Fimreite Software AS's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Fimreite Software AS in the registry?
The most recently registered devices listed for Fimreite Software AS include PACENTRIC CONNECT, TRAVELER AND WEB.