Endophotonix, Inc.
FDA 510(k) & PMA Approved Devices — 1 products
Advertisement
Total Devices1
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K082409 | SOLAR LASER ABLATION SYSTEM, MODELS: LU-1083-25, LF-1083, PC-1000, IC-1083, LW-2000, LG-2001, LK-001, PM-1083, TF-1083 | GEX | 2009-01-21 | View |
No matching devices.
Advertisement