Medical Device Manufacturer · US , Lake Forest , CA

Hemocue AB - FDA 510(k) Cleared Devices

6 submissions · 6 cleared · Since 2006

Total

Cleared

Denied

Hemocue AB has 6 FDA 510(k) cleared medical devices. Based in Lake Forest, US.

Historical record: 6 cleared submissions from 2006 to 2020. Primary specialty: Hematology.

Browse the FDA 510(k) cleared devices submitted by Hemocue AB Filter by specialty or product code using the sidebar.

FDA 510(k) cleared devices by Hemocue AB

6 devices

1-6 of 6