General Electric Medical Systems

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
6
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K052897GE DEFINIUM AMX 700, MODEL AMX 700November 8, 2005
K041521VOLUME VIEWER PLUSJune 22, 2004
K041270CT COLONOGRAPHY IIMay 27, 2004
K041267CARDIQ ANALYSIS IIIMay 27, 2004
K021780ADVANTAGE SIM 6.0July 29, 2002
K014058ENTEGRA PE PERSONAL DIGITAL ASSISTANTDecember 21, 2001