Shenzhen Urion Technology Co., Ltd.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 6
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K250046 | Air Compression Leg Massager (UM605, UM606, UM607, UM608,UM609,UM610, UM611, UM617) | April 25, 2025 |
| K243115 | Upper Arm Electronic Blood Pressure Monitor (U87Y series (models including U80Y, U81Y, U82Y,U83Y,U86 | February 21, 2025 |
| K241007 | Upper Arm Electronic Blood Pressure Monitor (U86E and TelliBP01) | October 24, 2024 |
| K200802 | Infrared Thermometer | October 7, 2020 |
| K160019 | U80 Series Upper Arm Electronic Blood Pressure Monitor | April 22, 2016 |
| K141683 | ELECTRONIC BLOOD PRESSURE MONITOR | April 3, 2015 |