FDA 510(k) Applications Submitted by Wondfo USA Co., Ltd.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K243256 | 10/15/2024 | WELLlifeÖ COVID-19 / Influenza A&B Home Test; WELLlifeÖ COVID-19 / Influenza A&B AntigenTest | Wondfo USA Co., Ltd. |
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