The O R Company Pty, Ltd.
FDA 510(k) & PMA Approved Devices — 2 products
Total Devices2
Categories1
Latest Approval2022-03-31
| Type | Number | Device Name | Code | Date | |
|---|---|---|---|---|---|
| 510(k) | K220202 | Uterine ElevatOR PRO with OccludOR Balloon | LKF | 2022-03-31 | View |
| 510(k) | K212505 | DUMI ManipulatOR | LKF | 2022-01-10 | View |
No matching devices.