Datex-Ohmeda - FDA 510(k) Cleared Devices
41
Total
41
Cleared
0
Denied
Datex-Ohmeda has 41 FDA 510(k) cleared medical devices. Based in Tewksbury, US.
Last cleared in 2023. Active since 2000. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Datex-Ohmeda Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Datex-Ohmeda
41 devices
Cleared
Dec 08, 2023
Novii+ Wireless Patch System
Obstetrics & Gynecology
158d
Cleared
Aug 08, 2013
GE DATEX-OHMEDA AVANCE CS2
Anesthesiology
42d
Cleared
Oct 12, 2012
AESPIRE 7900, AESPIRE VIEW
Anesthesiology
63d
Cleared
Sep 09, 2011
ENGSTROM CARESTATION, ENGSTROM PRO, MODELS 1505-9000-000, 1505-9003-000
Anesthesiology
141d
Cleared
Jun 06, 2007
GE DATEX-OHMEDA AVANCE ANESTHESIA SYSTEM
Anesthesiology
43d
Cleared
Jun 29, 2005
DATEX-OHMEDA OXY-AFR SENSOR
Anesthesiology
253d
Cleared
Feb 22, 2005
COMPATIBILITY ECG TRUNK CABLES
Cardiovascular
57d
Cleared
Feb 18, 2005
DATEX-OHMEDA S/5 PSM MODULE, (CONSISTING OF E-PSM AND E-PSMP MODULES) AND...
Cardiovascular
57d
Cleared
Dec 23, 2004
DATEX-OHMEDA S/5TM FM WITH L-FICU04 AND L-FICU04A SOFTWARE AND N-FCREC MODULE
Cardiovascular
27d
Cleared
Oct 15, 2004
GE DATEX-OHMEDA S/5 NETWORK AND ICENTRAL '03, SALES REVISION 3.3
Cardiovascular
10d
Cleared
Jul 28, 2004
DATEX-OHMEDA PRESTN.01 MODULE (MODEL FAMILY M-PRESTN.01) AND ACCESSORIES
Cardiovascular
27d
Cleared
Jul 23, 2004
DATEX-OHMEDA S/5 COMPACT ANESTHESIA MONITOR WITH L-CANE03 AND LCANE03A SOFTWARE
Cardiovascular
21d
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