Medical Device Manufacturer · US , Woodinville , WA

Oculus Optikgerate GmbH

6 submissions · 6 cleared · Since 2003
6
Total
6
Cleared
0
Denied

Oculus Optikgerate GmbH — FDA 510(k) Submissions

Oculus Optikgerate GmbH has submitted 6 FDA 510(k) premarket notifications since 2003, of which 6 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Device, Analysis, Anterior Segment, Tonometer, Ac-powered . Use the specialty filter in the sidebar to narrow results.

6 devices
1–6 of 6
Filters
Filter by Specialty
All6 Ophthalmic 6