Medical Device Manufacturer · NL , Amsterdam

Agendia - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 2009

Total

Cleared

Denied

Agendia has 3 FDA 510(k) cleared medical devices. Based in Amsterdam, NL.

Historical record: 3 cleared submissions from 2009 to 2015. Primary specialty: Pathology.

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

FDA 510(k) Regulatory Record - Agendia

3 devices

1-3 of 3