GEUDER INJECTOR FOR MORCHER CAPSULAR TENSION RING
Oct 2000
180d
Geuder GmbH
1
Total
1
Cleared
0
Denied
Geuder GmbH — FDA 510(k) Submissions
Geuder GmbH has submitted 1 FDA 510(k) premarket notifications since 2000, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Injector, Capsular Tension Ring . Use the specialty filter in the sidebar to narrow results.
1 devices