Leica Microsystems (Schweiz) AG is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Leica Microsystems (Schweiz) AG - FDA 510(k) Cleared Devices
Recent clearances: GLOW800
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: Neurology.
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) Regulatory Record - Leica Microsystems (Schweiz) AG
4 devices