Anhui Longway Medical Technology Co., Ltd.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 2
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K260642 | Manual Wheelchair (LW01108) | June 2, 2026 |
| K250366 | Electric Wheelchair (LW01301A07) | April 8, 2025 |