Sempulse Corporation - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Sempulse Corporation has 1 FDA 510(k) cleared medical devices. Based in San Marcos, US.
Latest FDA clearance: May 2024. Active since 2024. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Sempulse Corporation Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Sempulse Corporation
1 devices