Anuncia Medical, Inc.
FDA 510(k) & PMA Approved Devices — 2 products
Total Devices2
Categories1
Latest FDA decision2022-12-29
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K223603 | Reflow System Mini and ReFlow Mini Flusher | JXG | 2022-12-29 | View |
| 510(k) | K221918 | ReFlow System Mini | JXG | 2022-09-29 | View |
No matching devices.