Respironics Georgia, Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 2
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K011597 | SMARTMONITOR 2, MODEL 4000 | January 11, 2002 |
| K001708 | PROFOX SOFTWARE, MODEL 920M-41 | March 1, 2001 |