Beijing Demax Medical Technology Co.,Ltd
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 4
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K242248 | Introducer Sheath Kits | August 22, 2024 |
| K222184 | Introducer Sheath Kits | February 21, 2023 |
| K222182 | Radial Artery Compression Tourniquets | January 4, 2023 |
| K140943 | MASTRO PLUS BALLOON IN-DEFLATION DEVICE | March 5, 2015 |