LV Liberty Vision Model 1 90Yttrium Brachytherapy Source
May 2020
158d
Lv Liberty Vision Corporation
1
Total
1
Cleared
0
Denied
Lv Liberty Vision Corporation — FDA 510(k) Submissions
Lv Liberty Vision Corporation has submitted 1 FDA 510(k) premarket notifications since 2020, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Source, Brachytherapy, Radionuclide . Use the specialty filter in the sidebar to narrow results.
1 devices