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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-Number | Device | Date |
| K103730 | GE LUNAR VISCERAL FAT SOFTWARE | May 6, 2011 |
| K072664 | GE LUNAR FEMUR STRENGTH SOFTWARE | November 21, 2008 |
| K082185 | GE LOGIQ E9 DIAGNOSTIC ULTRASOUND SYSTEM, MODELS 5205000, 5205000-2 | August 15, 2008 |
| K073408 | GE LOGIQ BT08 DIAGNOSTIC ULTRASOUND SYSTEM | December 19, 2007 |
| K072439 | GE LUNAR DPX & PRODIGY SERIES DEXA BONE DENSITOMETERS WITH MOBILE KIT | September 14, 2007 |
| K052581 | LUNAR IDXA | October 20, 2005 |
| K041813 | GE LOGIQ 7 ULTRASOUND BT04 | July 23, 2004 |