Koo (Shanghai) Industries 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 |
|---|
| K112041 | KOO SMALL VOLUME NEBULIZER (SVN) | December 22, 2011 |
| K101136 | FISIO CHAMBER SPACE | January 28, 2011 |