Orion Corporation Soredex
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 4
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K983267 | DIGORA FOR WINDOWS 2.0 | December 30, 1998 |
| K974877 | CRANEX TOME CEPH, OR CRANEX TOME | March 27, 1998 |
| K934949 | DIGORA | February 10, 1994 |
| K880982 | ORALIX PAN DC III CEPH OR PANORAMIC MODE ONLY | June 6, 1988 |