Shenzhen Yimi Life-Technology Co., Ltd. is one of 1554 FDA 510(k) medical device manufacturers from China in the dataset, ranked by real submission volume.
Shenzhen Yimi Life-Technology Co., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: 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), Pulse Oximeter
2
Total
2
Cleared
0
Denied
Shenzhen Yimi Life-Technology Co., Ltd. has 2 FDA 510(k) cleared medical devices. Based in Shenzhen, CN.
Latest FDA clearance: Oct 2024. Active since 2019. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Shenzhen Yimi Life-Technology Co., Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Shenzhen Yimi Life Technology Co., Ltd. as regulatory consultant.
FDA 510(k) Regulatory Record - Shenzhen Yimi Life-Technology Co., Ltd.
2 devices