Agilent Technologies Deutschland GmbH - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
FDA 510(k) Regulatory Record - Agilent Technologies Deutschland GmbH Cardiovascular ✕
3 devices
Cleared
Feb 22, 2001
AGILENT COMPONENT MONITORING SYSTEM, AGILENT CARDIAC OUTPUT MODULE, AGILENT...
Cardiovascular
170d
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