Visionsense, Ltd.
FDA 510(k) & PMA Approved Devices — 4 products
Total Devices4
Categories3
Latest FDA decision2022-10-28
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K223020 | VS3-Iridium System (VS3-IR) | OWN | 2022-10-28 | View |
| 510(k) | K210265 | VS3 Iridium Sytem | OWN | 2021-11-22 | View |
| 510(k) | K171208 | Trans-anal Introducer | FED | 2018-02-05 | View |
| 510(k) | K153548 | VS3 STEREOSCOPIC HIGH DEFINITION VISION SYSTEM | HRX | 2016-02-22 | View |
No matching devices.