Daiken Medical 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 |
|---|
| K093888 | COOPDECH ENDOBRONCHIAL BLOCKER TUBE | March 16, 2010 |
| K071694 | COOPDECH ENDOBRONCHIAL BLOCKER TUBE, MODELS BBT-A30XXX, BBT-B30XXX | March 20, 2008 |