Ge Medical Systems Ultrasound and Primary Care Dia

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
7
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K103730GE LUNAR VISCERAL FAT SOFTWAREMay 6, 2011
K072664GE LUNAR FEMUR STRENGTH SOFTWARENovember 21, 2008
K082185GE LOGIQ E9 DIAGNOSTIC ULTRASOUND SYSTEM, MODELS 5205000, 5205000-2August 15, 2008
K073408GE LOGIQ BT08 DIAGNOSTIC ULTRASOUND SYSTEMDecember 19, 2007
K072439GE LUNAR DPX & PRODIGY SERIES DEXA BONE DENSITOMETERS WITH MOBILE KITSeptember 14, 2007
K052581LUNAR IDXAOctober 20, 2005
K041813GE LOGIQ 7 ULTRASOUND BT04July 23, 2004