Nk-Optik America is one of 6968 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Nk-Optik America - FDA 510(k) Cleared Devices
Recent clearances: LC-250 INFRARED LIGHT COAGULATOR
1
Total
1
Cleared
0
Denied
Nk-Optik America has 1 FDA 510(k) cleared medical devices. Based in Chicago, US.
Historical record: 1 cleared submissions from 1997 to 1997. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Nk-Optik America Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Nk-Optik America
1 devices