Remedi Co., Ltd.
FDA 510(k) & PMA Approved Devices — 3 products
Total Devices3
Categories3
Latest FDA decision2024-05-13
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K240759 | REMEX-GR100 | EHD | 2024-05-13 | View |
| 510(k) | K212144 | Remex KA6 | IZL | 2021-08-03 | View |
| 510(k) | K200284 | R-Sensor, R-Sensor | MUH | 2020-02-28 | View |
No matching devices.