Medical Device Manufacturer · NL , Amsterdam

Agendia BV - FDA 510(k) Cleared Devices

3 submissions · 2 cleared · Since 2007

Total

Cleared

Denied

Agendia BV has 2 FDA 510(k) cleared medical devices. Based in Amsterdam, NL.

Historical record: 2 cleared submissions from 2007 to 2008. Primary specialty: Pathology.

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

FDA 510(k) Regulatory Record - Agendia BV

3 devices

1-3 of 3