Somatex Medical Technologies GmbH
FDA 510(k) & PMA Approved Devices — 3 products
Total Devices3
Categories1
Latest FDA decision2021-02-18
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K201863 | Tumark Vision, Tumark Professional, Tumark Q, Tumark Professional Q-Shape | NEU | 2021-02-18 | View |
| 510(k) | K182082 | Tumark for Eviva, Tumark for Brevera | NEU | 2018-10-31 | View |
| 510(k) | K180443 | Tumark Vision | NEU | 2018-03-22 | View |
No matching devices.