EASY CONTROL MICRO INSERTER, MODEL ON385
Jul 2001
55d
Ophtec USA, Inc.
1
Total
1
Cleared
0
Denied
Ophtec USA, Inc. — FDA 510(k) Submissions
Ophtec USA, Inc. has submitted 1 FDA 510(k) premarket notifications since 2001, 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