Neteera Technologies , Ltd.
FDA 510(k) & PMA Approved Devices — 2 products
Total Devices2
Categories1
Latest FDA decision2024-02-09
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K231733 | Neteera 130H-Plus Vital Sign Monitoring Sensor | DRT | 2024-02-09 | View |
| 510(k) | K212143 | Neteera 130H/131H Vital Sign Monitoring Sensor | DRT | 2022-09-28 | View |
No matching devices.