Ge Medical Systems Information Technologies is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Ge Medical Systems Information Technologies - FDA 510(k) Cleared Devi...
Recent clearances: QT GUARD PLUS ANALYSIS SYSTEM, CARESCAPE MODEL V100 VITAL SIGNS MONITOR, 12SL ECG ANALYSIS PROGRAM
136
Total
132
Cleared
0
Denied
Ge Medical Systems Information Technologies has 132 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 132 cleared submissions from 1978 to 2012. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Ge Medical Systems Information Technologies Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Underwriters Laboratories, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Ge Medical Systems Information Technologies
136 devices
Cleared
Dec 06, 2012
QT GUARD PLUS ANALYSIS SYSTEM
Cardiovascular
267d
Cleared
Oct 20, 2010
CARESCAPE MODEL V100 VITAL SIGNS MONITOR
Cardiovascular
56d
Cleared
Feb 24, 2010
12SL ECG ANALYSIS PROGRAM
Cardiovascular
203d
Cleared
Dec 29, 2009
MARS HOLTER ANALYSIS WORKSTATION
Cardiovascular
85d
Cleared
Aug 28, 2009
CARESCAPE MONITOR B850
Cardiovascular
53d
Cleared
Apr 15, 2009
MODIFICATION TO DASH 2500 PATIENT MONITOR
Cardiovascular
29d
Cleared
Mar 23, 2009
CAPNOSTAT / CAPNOFLEX CO2 SYSTEM
Cardiovascular
96d
Cleared
Feb 17, 2009
MUSE CARDIOLOGY INFORMATION SYSTEM WITH VMWARE
Cardiovascular
70d
Cleared
Nov 19, 2008
MULTLINK CABLE AND LEADWIRE SYSTEM
Cardiovascular
51d
Cleared
Jul 15, 2008
MAC 1600 ECG ANALYSIS SYSTEM
Cardiovascular
54d
Cleared
Jun 20, 2008
APEXPRO TELEMETRY SYSTEMS
Cardiovascular
141d
Cleared
Mar 24, 2008
DASH 2500 PATIENT MONITOR
Cardiovascular
61d
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