Pneumowave, Ltd. - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Pneumowave, Ltd. has 1 FDA 510(k) cleared medical devices. Based in Eurocentral, GB.
Latest FDA clearance: Apr 2025. Active since 2025. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Pneumowave, Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Pneumowave, Ltd.
1 devices