Hortmann AG
FDA 510(k) & PMA Approved Devices — 2 products
Advertisement
Total Devices2
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K994033 | HORTMANN ECHOMASTER OAE ANALYZER | EWO | 2000-02-24 | View |
| 510(k) | K980505 | HORTMANN AMDIS-OAE OAE ANALYZER | EWO | 1998-04-07 | View |
No matching devices.
Advertisement