Qingdao Hisense Medical Equipment Co., Ltd.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 9
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
| K233841 | HD80 Series Ultrasound Diagnostic System | May 16, 2024 |
| K233439 | HD60 Series Ultrasound Diagnostic System | February 21, 2024 |
| K222208 | Hisense LCD monitor HMD2C21A, HMD4C27S, HMD6C30D | November 17, 2022 |
| K222132 | Hisense LCD monitor HMD2G21S, HMD3G21S | November 8, 2022 |
| K221567 | LCD monitor (HMD3C21S), LCD monitor (HMD5G21S) | July 26, 2022 |
| K213862 | HD60 Series Ultrasound Diagnostic System | June 8, 2022 |
| K160347 | Hisense LDC monitor models HMD2G21/HMD3G21/HMD5G21 | March 3, 2016 |
| K152030 | Hisense 2MP/3MP LCD Monitor (HMD2C21/HMD3C21) | September 16, 2015 |
| K151709 | Hi-Light Diagnostic Ultrasound Systems | July 17, 2015 |