Agilent Technologies - FDA 510(k) Cleared Devices
13
Total
13
Cleared
0
Denied
Agilent Technologies has 13 FDA 510(k) cleared cardiovascular devices. Based in Walker, US.
Historical record: 13 cleared submissions from 1982 to 2001.
Browse the complete list of FDA 510(k) cleared cardiovascular devices from this manufacturer. Filter by specialty or product code using the sidebar.
13 devices
Cleared
Sep 28, 2001
2010 PLUS HOLTER FOR WINDOWS
Cardiovascular
183d
Cleared
Feb 08, 2001
2010 PLUS HOLTER FOR WINDOWS
Cardiovascular
49d
Cleared
Jan 05, 2001
2010 PLUS HOLTER FOR WINDOWS
Cardiovascular
30d
Cleared
May 17, 2000
MODIFICATION TO ZYMED TELEMETRY SYSTEM, MODEL EASIVIEW
Anesthesiology
22d
Cleared
May 11, 1999
ZYMED TELEMETRY SYSTEM: MODEL EASIVIEW
Cardiovascular
120d
Cleared
Oct 07, 1998
ZYMED TELEMETRY SYSTEM
Cardiovascular
260d
Cleared
Jan 24, 1995
DIGITAL HOLTER RECORDER
Cardiovascular
225d
Cleared
Apr 25, 1994
ZYMED HOLTER SCANNER MODEL 2010
Cardiovascular
433d
Cleared
Dec 15, 1992
ZYMED TELEMETRY MONITOR MODEL T8010 (PRELIMINARY)
Cardiovascular
90d
Cleared
Dec 12, 1989
ZYMED MODEL 1610
Cardiovascular
117d
Cleared
Feb 07, 1985
QUIKPAGE ARRHYTHMIA REPORT GENERATOR
Cardiovascular
331d
Cleared
Nov 03, 1982
HOLTER RECORDER
Cardiovascular
26d
Cleared
Sep 21, 1982
QUIKPAGE SCANNER
Cardiovascular
27d