Irras USA is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Irras USA - FDA 510(k) Cleared Devices
Recent clearances: IRRAflow Active Fluid Exchange System (AFES)
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) Regulatory Record - Irras USA
1 devices