Agilent Technologies Deutschland GmbH is one of 234 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
Agilent Technologies Deutschland GmbH - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Agilent Technologies Deutschland GmbH has 4 FDA 510(k) cleared medical devices. Based in Boeblingen,, DE.
Historical record: 4 cleared submissions from 2000 to 2001. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Agilent Technologies Deutschland GmbH Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Agilent Technologies Deutschland GmbH
4 devices
Cleared
Feb 22, 2001
AGILENT COMPONENT MONITORING SYSTEM, AGILENT CARDIAC OUTPUT MODULE, AGILENT...
Cardiovascular
170d
Cleared
Dec 15, 2000
AGILENT COMPONENT MONITORING SYSTEM, AGILENT V24/26, AGILENT BIS MODULE,...
Neurology
77d
Cleared
Jun 30, 2000
AGILENT COMPONENT MONITORING SYSTEM
Cardiovascular
24d
Cleared
May 17, 2000
AGILENT COMPONENT MONITORING SYSTEM, AGILENT MULTI-MEASUREMENT SERVER AND...
Cardiovascular
20d