Scopis GmbH
FDA 510(k) & PMA Approved Devices — 2 products
Total Devices2
Categories1
Latest FDA decision2017-09-27
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K171661 | Scopis Extended Instrument Set EM | PGW | 2017-09-27 | View |
| 510(k) | K161491 | Scopis Hybrid Navigation System EM | PGW | 2017-02-09 | View |
No matching devices.