Pulmone Advanced Medical Devices, Ltd.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 3
- Inspections
- 1
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K161295 | MiniBox + | October 21, 2016 |
| K141793 | PULMONE MINIBOXPFT 2.0 | March 6, 2015 |
| K133051 | PULMONE MINIBOX PFT TM | May 2, 2014 |