Leadtek Research, Inc.
FDA 510(k) & PMA Approved Devices — 2 products
Total Devices2
Categories1
Latest Approval2021-09-01
| Type | Number | Device Name | Code | Date | |
|---|---|---|---|---|---|
| 510(k) | K210032 | Leadtek Fingertip Pulse Oximeter (Wireless), Leadtek Fingertip Pulse Oximeter (Wireless) | DQA | 2021-09-01 | View |
| 510(k) | K193350 | Leadtek Fingertip Pulse Oximeter | DQA | 2020-04-27 | View |
No matching devices.