Ardent Production Development
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 2
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
| K964192 | ARDENT NON GAMMA-2 70 | January 6, 1997 |
| K964775 | ARDENT FUTURA NON GAMMA-2 | December 10, 1996 |