Qserve America, Inc.
FDA 510(k) & PMA Approved Devices — 2 products
Advertisement
Total Devices2
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K123514 | CLEARPATH ALIGNER | NXC | 2013-11-01 | View |
| 510(k) | K110246 | MEDISIZE RED AND MEDISIZE BLUE | CAH | 2011-11-04 | View |
No matching devices.
Advertisement