Wondfo USA Co, Ltd.
FDA 510(k) & PMA Approved Devices — 2 products
Total Devices2
Categories1
Latest FDA decision2025-08-20
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K251563 | WELLlife Flu A&B Home Test; WELLlife Influenza A&B Test | SCA | 2025-08-20 | View |
| 510(k) | K243256 | WELLlife™ COVID-19 / Influenza A&B Home Test; WELLlife™ COVID-19 / Influenza A&B AntigenTest | SCA | 2025-01-16 | View |
No matching devices.