Leica Microsystems (Schweiz) AG - FDA 510(k) Cleared Devices
4
Total
2
Cleared
1
Denied
Leica Microsystems (Schweiz) AG has 2 FDA 510(k) cleared medical devices. Based in Orange, US.
Historical record: 2 cleared submissions from 2008 to 2018. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Leica Microsystems (Schweiz) AG Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Leica Microsystems (Schweiz) AG
4 devices