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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