Ge Medical Systems Ultrasound and Primary Care Dia
FDA 510(k) & PMA Approved Devices — 7 products
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Total Devices7
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K103730 | GE LUNAR VISCERAL FAT SOFTWARE | KGI | 2011-05-06 | View |
| 510(k) | K072664 | GE LUNAR FEMUR STRENGTH SOFTWARE | KGI | 2008-11-21 | View |
| 510(k) | K082185 | GE LOGIQ E9 DIAGNOSTIC ULTRASOUND SYSTEM, MODELS 5205000, 5205000-2 | IYO | 2008-08-15 | View |
| 510(k) | K073408 | GE LOGIQ BT08 DIAGNOSTIC ULTRASOUND SYSTEM | IYN | 2007-12-19 | View |
| 510(k) | K072439 | GE LUNAR DPX & PRODIGY SERIES DEXA BONE DENSITOMETERS WITH MOBILE KIT | KGI | 2007-09-14 | View |
| 510(k) | K052581 | LUNAR IDXA | KGI | 2005-10-20 | View |
| 510(k) | K041813 | GE LOGIQ 7 ULTRASOUND BT04 | IYN | 2004-07-23 | View |
No matching devices.
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