Shenzhen Imdk Medical Technology Co., Ltd.
Shenzhen Imdk Medical Technology Co., Ltd. holds FDA 510(k) medical device clearances, first cleared 2018, most recent 2026.
Top product codes for Shenzhen Imdk Medical Technology Co., Ltd.
Recent clearances by Shenzhen Imdk Medical Technology Co., Ltd.
- K252655 — Pulse Oximeter (PO-A2AO, PO-A2AT, PO-A3AO, PO-H1AO, PO-B1AO, PO-C5AO, PO-C5AT, PO-C6AO, PO-C6AT)
- K253133 — Wrist Blood Pressure Monitor (BPM-W1VL)
- K243118 — Arm Blood Pressure Monitor (model: BPM-A7VL)
- K233040 — EMS/TENS Massager Device
- K221979 — Pulse Oximeter (Model C101A2, C101B1, C101A3)
- K173123 — Pulse Oximeter
- K180419 — Ultrasonic Doppler (Model YM-2T8)
Data sourced from openFDA. This site is unofficial and independent of the FDA.