Deepwell Dtx, Inc. - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Deepwell Dtx, Inc. has 1 FDA 510(k) cleared medical devices. Based in Seattle, US.
Latest FDA clearance: Aug 2024. Active since 2024. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Deepwell Dtx, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Deepwell Dtx, Inc.
1 devices