Neauvia North America, Inc.
FDA 510(k) & PMA Approved Devices — 3 products
Total Devices3
Categories1
Latest FDA decision2023-01-17
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K223222 | Plasma IQ | GEI | 2023-01-17 | View |
| 510(k) | K212329 | Plasma IQ | GEI | 2021-12-09 | View |
| 510(k) | K192813 | Plasma IQ | GEI | 2020-03-06 | View |
No matching devices.