Optovue, Inc.
FDA 510(k) & PMA Approved Devices — 15 products
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Total Devices15
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 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 |
| 510(k) | K130656 | IFUSION | HKI | 2013-07-03 | View |
| 510(k) | K121739 | IVUE WITH NORMATIVE DATABASE | HLI | 2013-01-18 | View |
| 510(k) | K122572 | ICAM FUNDUS CAMERA | HKI | 2013-01-11 | View |
| 510(k) | K120238 | RTVUE XR OCT | HLI | 2012-04-03 | View |
| 510(k) | K111505 | RTVUE CAM WITH CORNEAL POWER UPGRADE | OBO | 2011-09-08 | View |
| 510(k) | K103266 | ISTAND | HLI | 2011-06-03 | View |
| 510(k) | K101505 | RTVUE MODEL RTVUE 100 | HLI | 2010-09-15 | View |
| 510(k) | K100861 | R T VUE WITH SOFTWARE 5.0 MODEL: R I VUE 100 | HLI | 2010-06-17 | View |
| 510(k) | K091404 | IVUE, MODEL 100 | OBO | 2010-04-22 | View |
| 510(k) | K071250 | CA, MODEL: CAM | OBO | 2007-09-28 | View |
| 510(k) | K062552 | RTVUE | OBO | 2006-10-06 | View |
No matching devices.
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