Apriomed AB
FDA 510(k) & PMA Approved Devices — 2 products
Total Devices2
Categories2
Latest FDA decision2020-02-27
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K193268 | APrioCore Plus | KNW | 2020-02-27 | View |
| 510(k) | K181756 | Gangi-SoftGuard Coaxial Needle, Gangi-HydroGuard Coaxial Needle | FCG | 2018-12-18 | View |
No matching devices.