Visionsense, Ltd.
FDA 510(k) & PMA Approved Devices — 10 products
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Total Devices10
Categories0
Latest FDA decision
| 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 |
| 510(k) | K131434 | VS3 STEREOSCOPIC HIGH DEFINITION VISION SYSTEM | GWG | 2013-07-16 | View |
| 510(k) | K123467 | VS3 | GCJ | 2013-04-17 | View |
| 510(k) | K082355 | VISIONSENSE STEREOSCOPIC VISION SYSTEM | HRX | 2008-12-15 | View |
| 510(k) | K082667 | VISIONSENSE STEREOSCOPIC VISION SYSTEM (VS SYSTEM) | EOB | 2008-10-30 | View |
| 510(k) | K081102 | VSU - VISIONSENSE STEREOSCOPIC VISION SYSTEM | GWG | 2008-05-29 | View |
| 510(k) | K073279 | VS-VISIONSENSE STEREOSCOPIC VISION SYSTEM | GCJ | 2008-03-05 | View |
No matching devices.
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