Acare Technology Co., Ltd.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 2
- Inspections
- 2
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K182950 | Acare Suction Unit | August 23, 2019 |
| K111617 | PULSE OXIMETER MODEL AB-F1/AH-S1/AH-M1 | December 22, 2011 |