Ge Medical Systems Ultrasound and Primary Care Dia is one of 16306 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Ge Medical Systems Ultrasound and Primary Care Dia - FDA 510(k) Clear...
Recent clearances: GE LUNAR VISCERAL FAT SOFTWARE, GE LUNAR FEMUR STRENGTH SOFTWARE, GE LOGIQ E9 DIAGNOSTIC ULTRASOUND SYSTEM, MODELS 5205000, 5205000-2
7
Total
7
Cleared
0
Denied
Ge Medical Systems Ultrasound and Primary Care Dia has 7 FDA 510(k) cleared medical devices. Based in Milwaukee, US.
Historical record: 7 cleared submissions from 2004 to 2011. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Ge Medical Systems Ultrasound and Primary Care Dia Filter by specialty or product code using the sidebar.
1 device has linked clinical trial registered on ClinicalTrials.gov.
FDA 510(k) Regulatory Record - Ge Medical Systems Ultrasound and Primary Care Dia
7 devices
Cleared
CT
May 06, 2011
GE LUNAR VISCERAL FAT SOFTWARE
Radiology
136d
Cleared
Nov 21, 2008
GE LUNAR FEMUR STRENGTH SOFTWARE
Radiology
428d
Cleared
Aug 15, 2008
GE LOGIQ E9 DIAGNOSTIC ULTRASOUND SYSTEM, MODELS 5205000, 5205000-2
Radiology
14d
Cleared
Dec 19, 2007
GE LOGIQ BT08 DIAGNOSTIC ULTRASOUND SYSTEM
Radiology
15d
Cleared
Sep 14, 2007
GE LUNAR DPX & PRODIGY SERIES DEXA BONE DENSITOMETERS WITH MOBILE KIT
Radiology
15d
Cleared
Oct 20, 2005
LUNAR IDXA
Radiology
30d
Cleared
Jul 23, 2004
GE LOGIQ 7 ULTRASOUND BT04
Radiology
17d