Medical Device Manufacturer · US , Gendale , CA

Oculab, Inc. - FDA 510(k) Cleared Devices

7 submissions · 7 cleared · Since 1985

Total

Cleared

Denied

Oculab, Inc. has 7 FDA 510(k) cleared medical devices. Based in Gendale, US.

Historical record: 7 cleared submissions from 1985 to 1989. Primary specialty: Ophthalmic.

Browse the FDA 510(k) cleared devices submitted by Oculab, Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Oculab, Inc.

7 devices

1-7 of 7