Medical Device Manufacturer · US , Irvina , CA

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

2 submissions · 2 cleared · Since 2020

Total

Cleared

Denied

Agendia, Inc. has 2 FDA 510(k) cleared medical devices. Based in Irvina, US.

Last cleared in 2022. Active since 2020. Primary specialty: Pathology.

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

FDA 510(k) cleared devices by Agendia, Inc.

2 devices

1-2 of 2