Osypka AG - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Osypka AG has 1 FDA 510(k) cleared medical devices. Based in Rheinfelden, DE.
Latest FDA clearance: Apr 2024. Active since 2024. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Osypka AG Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Osypka AG
1 devices