Harps Europe Manufacturing GmbH - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Harps Europe Manufacturing GmbH has 1 FDA 510(k) cleared medical devices. Based in Niederosterreich, AT.
Latest FDA clearance: Aug 2025. Active since 2025. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Harps Europe Manufacturing GmbH Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Harps Europe Manufacturing GmbH
1 devices