Somnomedics GmbH - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
Somnomedics GmbH has 7 FDA 510(k) cleared medical devices. Based in Washington, US.
Latest FDA clearance: Dec 2024. Active since 2007. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Somnomedics GmbH Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Somnomedics GmbH
7 devices
Cleared
Dec 08, 2024
HomeSleepTest (HST, HST REM+)
Neurology
269d
Cleared
Nov 27, 2023
ABPMpro
Cardiovascular
222d
Cleared
Jun 15, 2022
EEG-acp
Neurology
324d
Cleared
Aug 12, 2020
SOMNOscreen plus
Neurology
113d
Cleared
Jan 30, 2015
SOMNOTOUCH RESP
Anesthesiology
302d
Cleared
Sep 18, 2008
SOMNOWATCH
Anesthesiology
113d
Cleared
Jul 18, 2007
SOMNOSCREEN EEG10-20
Anesthesiology
41d