Optovue, Inc.
FDA 510(k) & PMA Approved Devices — 4 products
Total Devices4
Categories2
Latest Approval2022-11-09
| Type | Number | Device Name | Code | Date | |
|---|---|---|---|---|---|
| 510(k) | K222166 | SOLIX | OBO | 2022-11-09 | View |
| 510(k) | K180660 | Avanti | OBO | 2018-06-08 | View |
| 510(k) | K163475 | iVue | OBO | 2017-06-09 | View |
| 510(k) | K153080 | RTVue XR OCT Avanti with AngioVue Software | HLI | 2016-02-11 | View |
No matching devices.