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.

Hemocue AB is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Hemocue AB

6 devices

1-6 of 6