Medical Device Manufacturer · US , San Diego , CA

Irras USA - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2022

1

Total

1

Cleared

0

Denied

Irras USA has 1 FDA 510(k) cleared medical devices. Based in San Diego, US.

Last cleared in 2022. Active since 2022. Primary specialty: Neurology.

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

FDA 510(k) cleared devices by Irras USA

1 devices

1-1 of 1

Cleared Dec 08, 2022

IRRAflow Active Fluid Exchange System (AFES)

Neurology · 114d