Xvivo Perfusion AB is one of 59 FDA 510(k) medical device manufacturers from Sweden in the dataset, ranked by real submission volume.
Xvivo Perfusion AB - FDA 510(k) Cleared Devices
Recent clearances: KIDNEY ASSIST-transport, Perfadex Plus
3
Total
3
Cleared
0
Denied
Xvivo Perfusion AB has 3 FDA 510(k) cleared medical devices. Based in Gutengurg, SE.
Last cleared in 2022. Active since 2010. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Xvivo Perfusion AB Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Medical Device Approvals, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Xvivo Perfusion AB
3 devices