Getemed Medizin- Und Informationstechnik AG
FDA 510(k) & PMA Approved Devices — 8 products
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Total Devices8
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K162023 | CardioDay V2.5 | DQK | 2017-03-24 | View |
| 510(k) | K130516 | CARDIODAY | DQK | 2013-08-23 | View |
| 510(k) | K130785 | SEER 1000 | MWJ | 2013-07-26 | View |
| 510(k) | K122272 | CARDIOMEM | MWJ | 2013-03-28 | View |
| 510(k) | K063042 | CARDIOMEM CM 3000-12BT | MWJ | 2007-05-30 | View |
| 510(k) | K070280 | CARDIODAY, VERSION 2.0 | DQK | 2007-02-23 | View |
| 510(k) | K051686 | CARDIOMEM CM 3000-12 | MWJ | 2005-07-14 | View |
| 510(k) | K051471 | CARDIODAY | DQK | 2005-06-29 | View |
No matching devices.
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