Perimed AB is one of 59 FDA 510(k) medical device manufacturers from Sweden in the dataset, ranked by real submission volume.
Perimed AB - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Perimed AB has 4 FDA 510(k) cleared medical devices. Based in Jarfalla, SE.
Historical record: 4 cleared submissions from 2001 to 2016. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Perimed AB Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Perimed AB
4 devices