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Guangzhou Homesun 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 |
| K231561 | Pulmonary Function Tester, Model: A9 | February 21, 2024 |
| K191239 | Smart Peak Flow Meter | December 6, 2019 |