Lasertek OY is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Lasertek OY - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Lasertek OY has 4 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 4 cleared submissions from 1979 to 1984. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Lasertek OY Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Lasertek OY
4 devices