Avantis Medical Systems, Inc.
FDA 510(k) & PMA Approved Devices — 5 products
Advertisement
Total Devices5
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K160356 | Third Eye Panoramic Auxiliary Endoscopy System - Resposable | FDF | 2016-05-17 | View |
| 510(k) | K093187 | MODIFICATION TO THIRD EYE RETROSCOPE AUXILIARY ENDOSCOPY SYSTEM | FDF | 2009-11-05 | View |
| 510(k) | K091783 | THIRD EYE RETROSCOPE AUXILIARY ENDOSCOPE SYSTEM | FDF | 2009-07-07 | View |
| 510(k) | K083180 | THIRD EYE RETROSCOPE AUXILIARY ENDOSCOPY SYSTEM | FDF | 2009-02-12 | View |
| 510(k) | K070330 | THIRD EYE RETROSCOPE AUXILIARY ENDOSCOPY SYSTEM | FDF | 2007-04-24 | View |
No matching devices.
Advertisement