Auris Surgical Robotics, Inc.
FDA 510(k) & PMA Approved Devices — 2 products
Total Devices2
Categories1
Latest FDA decision2018-03-22
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K173760 | Monarch Endoscopy Platform (Monarch Platform) | EOQ | 2018-03-22 | View |
| 510(k) | K152319 | Auris Robotic Endoscopy System (ARES) | EOQ | 2016-05-26 | View |
No matching devices.