Company ยท US
Getemed Medizin- Und Informationstechnik AG
FDA 510(k) clearances and medical device recalls filed under this name, 2005 to 2017. Name variants (Inc, Corp, punctuation) are merged.
8510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Mar 24, 2017 | K162023 | CardioDay V2.5 Getemed Medizin- Und Informationstechnik AG, DE | DQK |
| Aug 23, 2013 | K130516 | CARDIODAY Getemed Medizin- Und Informationstechnik AG, DE | DQK |
| Jul 26, 2013 | K130785 | SEER 1000 Getemed Medizin- Und Informationstechnik AG, DE | MWJ |
| Mar 28, 2013 | K122272 | CARDIOMEM Getemed Medizin- Und Informationstechnik AG | MWJ |
| May 30, 2007 | K063042 | CARDIOMEM CM 3000-12BT Getemed Medizin- Und Informationstechnik AG | MWJ |
| Feb 23, 2007 | K070280 | CARDIODAY, VERSION 2.0 Getemed Medizin- Und Informationstechnik AG | DQK |
| Jul 14, 2005 | K051686 | CARDIOMEM CM 3000-12 Getemed Medizin- Und Informationstechnik AG | MWJ |
| Jun 29, 2005 | K051471 | CARDIODAY Getemed Medizin- Und Informationstechnik AG | DQK |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||