Nam illumination probe with chopper
Aug 2021
340d
Oculight , Ltd.
1
Total
1
Cleared
0
Denied
Oculight , Ltd. — FDA 510(k) Submissions
Oculight , Ltd. has submitted 1 FDA 510(k) premarket notifications since 2021, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Endoilluminator . Use the specialty filter in the sidebar to narrow results.
1 devices