Xtreem Pulse, LLC - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Xtreem Pulse, LLC has 4 FDA 510(k) cleared medical devices. Based in New York, US.
Latest FDA clearance: Mar 2025. Active since 2018. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Xtreem Pulse, LLC Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Xtreem Pulse, LLC
4 devices