Shenzhen Witleaf Medical Electronics Co., Ltd.
FDA 510(k) & PMA Approved Devices — 2 products
Total Devices2
Categories1
Latest FDA decision2023-02-26
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K213431 | Handheld Pulse Oximeter | DQA | 2023-02-26 | View |
| 510(k) | K213430 | Fingertip Pulse Oximeter | DQA | 2022-12-30 | View |
No matching devices.