Ge Dec Medical Systems
FDA 510(k) & PMA Approved Devices — 10 products
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Total Devices10
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K000221 | SERIES 7700 MOBILE C-ARM, COMPACT 7700 MOBILE C-ARM, COMPACT 7700 PLUS MOBILE C-ARM | OWB | 2000-04-11 | View |
| 510(k) | K993687 | UROVIEW 2800 | OWB | 1999-12-21 | View |
| 510(k) | K992506 | MINI 6800 DIGITAL MOBILE C-ARM | OXO | 1999-08-19 | View |
| 510(k) | K974355 | INTERVENTIONAL MOBILE DIGITAL IMAGING SYSTEM (HEREIN CALLED IMDIS) | OWB | 1998-02-17 | View |
| 510(k) | K970063 | SERIES 7600 MOBILE DIGITAL C-ARM | OWB | 1997-03-11 | View |
| 510(k) | K963952 | SERIES 9600 MOBILE DIGITAL IMAGING SYSTEM | OWB | 1996-12-23 | View |
| 510(k) | K950781 | COMPACT 7600 | JAA | 1995-06-05 | View |
| 510(k) | K951765 | SERIES 6600 DIGITAL MOBILE C-ARM | OXO | 1995-05-11 | View |
| 510(k) | K940295 | UROVIEW MODEL 2600 | JAA | 1994-08-22 | View |
| 510(k) | K936136 | UROVIEW SYSTEMS TOMOGRAPHY OPTION SOFTWARE | JAA | 1994-01-25 | View |
No matching devices.
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