Getemed Medizin- Und Informationstechnik AG
Getemed Medizin- Und Informationstechnik AG appears in FDA public data with 0 recalls, 8 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on March 24, 2017.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 8
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K162023 | CardioDay V2.5 | March 24, 2017 |
| K130516 | CARDIODAY | August 23, 2013 |
| K130785 | SEER 1000 | July 26, 2013 |
| K122272 | CARDIOMEM | March 28, 2013 |
| K063042 | CARDIOMEM CM 3000-12BT | May 30, 2007 |
| K070280 | CARDIODAY, VERSION 2.0 | February 23, 2007 |
| K051686 | CARDIOMEM CM 3000-12 | July 14, 2005 |
| K051471 | CARDIODAY | June 29, 2005 |