Oasis Lacrimal Intubation Set
May 2016
59d
Anodyne
1
Total
0
Cleared
0
Denied
Anodyne — FDA 510(k) Submissions
Anodyne has submitted 1 FDA 510(k) premarket notifications since 2016, of which 0 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Lacrimal Stents And Intubation Sets . Use the specialty filter in the sidebar to narrow results.
1 devices