Medical Device Manufacturer · US , Mchenry , IL

Lasertek OY - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 1979

Total

Cleared

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

1-4 of 4