Apriomed AB is one of 59 FDA 510(k) medical device manufacturers from Sweden in the dataset, ranked by real submission volume.
Apriomed AB - FDA 510(k) Cleared Devices
Recent clearances: APrioCore Plus, Gangi-SoftGuard Coaxial Needle, Gangi-HydroGuard Coaxial Needle
3
Total
3
Cleared
0
Denied
Apriomed AB has 3 FDA 510(k) cleared medical devices. Based in Uppsala, SE.
Historical record: 3 cleared submissions from 2015 to 2020. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Apriomed AB Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Apriomed AB
3 devices