MaxiTears Contacts PF
Jul 2019
268d
Omnivision AG
1
Total
1
Cleared
0
Denied
Omnivision AG — FDA 510(k) Submissions
Omnivision AG has submitted 1 FDA 510(k) premarket notifications since 2019, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Products, Contact Lens Care, Rigid Gas Permeable . Use the specialty filter in the sidebar to narrow results.
1 devices