Agilent Technologies, Inc. - FDA 510(k) Cleared Devices
30
Total
30
Cleared
0
Denied
24 devices
Cleared
Jul 20, 2001
MODIFICATION TO DEVICE LINK SYSTEM, MODEL M2376A
Cardiovascular
15d
Cleared
Jul 02, 2001
AGILENT M2636B TELEMON B MONITOR (TELEMON B)
Cardiovascular
21d
Cleared
Jun 11, 2001
HEARTSTREAM XL DEFIBIBRILLATOR/MONITOR, MODEL M4735A, HEARTSTREAM XLT...
Cardiovascular
101d
Cleared
Jun 08, 2001
M2376A DEVICELINK SYSTEM, MODEL M2376A
Cardiovascular
17d
Cleared
May 02, 2001
HEARTSTREAM ATTENUATED DEFIBRILLATION PADS, MODEL M3870A
Cardiovascular
142d
Cleared
May 01, 2001
AGILENT INFORMATION CENTER SOFTWARE FOR M3150,M3151,M3153 AND M3154
Cardiovascular
21d
Cleared
Mar 02, 2001
M2376A DEVICELINK SYSTEM
Cardiovascular
15d
Cleared
Feb 14, 2001
M2376A DEVICELINK SYSTEM, MODEL M2376A
Cardiovascular
9d
Cleared
Feb 01, 2001
M2376A DEVICELINK SYSTEM
Cardiovascular
27d
Cleared
Dec 20, 2000
HEARTSTREAM FR2 AED, MODEL M3860A,M3861A
Cardiovascular
30d
Cleared
Dec 20, 2000
ST/AR ST AND ARRHYTHMIA SOFTWARE, MODEL RELEASE D.0
Cardiovascular
26d
Cleared
Dec 18, 2000
M2376A DEVICELINK SYSTEM, MODEL M2376A
Cardiovascular
24d