Sempulse Corporation is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Sempulse Corporation - FDA 510(k) Cleared Devices
Recent clearances: Sempulse Halo Vital Signs Monitor
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) Regulatory Record - Sempulse Corporation
1 devices