FDA 510(k) Applications Submitted by LI Medical Corporation Ltd.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K240364 | 02/06/2024 | RELIEEV Uterine Manipulator Injector (CUMI 5.0) | LI Medical Corporation Ltd. |
| K240434 | 02/14/2024 | RELIEEV Suction Curette (Flexible 3.0/ Standard 3.6) | Li Medical Corporation Ltd. |
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