Berkeley VC-10 Vacuum Curettage System
Sep 2017
136d
Gyrus Acmi
1
Total
1
Cleared
0
Denied
Gyrus Acmi — FDA 510(k) Submissions
Gyrus Acmi has submitted 1 FDA 510(k) premarket notifications since 2017, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include System, Abortion, Vacuum . Use the specialty filter in the sidebar to narrow results.
1 devices