Campomats S.r.l.
ItalyFDA applicant, unverified
- Devices
- 1
What Campomats S.r.l. makes
Campomats S.R.L. makes the 1NEED Pro device.
The 1NEED Pro is a Class II medical device listed in the FDA 510(k) registry, and the company is based in the United States.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
1NEED Pro Ref K243472
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Campomats S.R.L. have in the registry?
The registry currently lists 1 device for Campomats S.R.L.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Campomats S.R.L.'s devices?
Among its 1 most recently registered device, Campomats S.R.L. has devices listed in FDA 510(k) (1 device).
What risk classes do Campomats S.R.L.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Campomats S.R.L.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Campomats S.R.L. in the registry?
The most recently registered devices listed for Campomats S.R.L. include 1NEED Pro.