LV Liberty Vision
Also registered as Lv Liberty Vision Corp., Lv Liberty Vision Corporation
United Statesfrom the FDA registration address FDA establishment FEI 3015042204
- Devices
- 2
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3015042204
- Address
- 300 West Rd Ste 2, Portsmouth, NH, 03801
Frequently asked questions
How many devices does LV Liberty Vision have in the registry?
The registry currently lists 2 devices for LV Liberty Vision. Devices recorded under merged duplicate company entries are counted once.
Which registries list LV Liberty Vision's devices?
Among its 2 most recently registered devices, LV Liberty Vision has devices listed in FDA 510(k) (2 devices).
What risk classes do LV Liberty Vision's devices fall under?
Among its 2 most recently registered devices, the classes recorded for LV Liberty Vision's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from LV Liberty Vision in the registry?
The most recently registered devices listed for LV Liberty Vision include LV Liberty Vision Model 1 90Yttrium Brachytherapy Source and LV Liberty Vision Model 1 90 Yttrium Brachytherapy Source.