Sichuan Ast Medical Equipment Co., Ltd.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 3
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K242722 | Manual Wheelchair (MASY23) | November 22, 2024 |
| K231750 | MA012 Aluminum wheelchair, MS019 steel wheelchair | August 15, 2023 |
| K181795 | AST Model MA012 and MS019 Rehab Wheelchair | September 25, 2018 |