Shenzhen Imdk Medical Technology Co., Ltd.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 7
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K252655 | Pulse Oximeter (PO-A2AO, PO-A2AT, PO-A3AO, PO-H1AO, PO-B1AO, PO-C5AO, PO-C5AT, PO-C6AO, PO-C6AT) | May 11, 2026 |
| K253133 | Wrist Blood Pressure Monitor (BPM-W1VL) | February 13, 2026 |
| K243118 | Arm Blood Pressure Monitor (model: BPM-A7VL) | November 26, 2024 |
| K233040 | EMS/TENS Massager Device | February 12, 2024 |
| K221979 | Pulse Oximeter (Model C101A2, C101B1, C101A3) | October 16, 2022 |
| K173123 | Pulse Oximeter | August 13, 2018 |
| K180419 | Ultrasonic Doppler (Model YM-2T8) | July 19, 2018 |