FDA 510(k) Applications Submitted by Shenzhen Yimi Life Technology Co., Ltd.
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K240092 |
01/12/2024 |
Pulse Oximeter (YM101, YM102, YM103, YM104, YM201, YM301, YM202, YM302, YM111, YM112, YM113, YM114, YM211, YM212, YM314, YM601, YM602, YM401, YM402, YM403, YM501, YM502, YM503 and YM504) |
Shenzhen Yimi Life Technology Co., Ltd. |
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