Lisca Development AB is one of 59 FDA 510(k) medical device manufacturers from Sweden in the dataset, ranked by real submission volume.
Lisca Development AB - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Lisca Development AB has 1 FDA 510(k) cleared medical devices. Based in Linkoping, SE.
Historical record: 1 cleared submissions from 1992 to 1992. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Lisca Development AB Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Lisca Development AB
1 devices