Compagnie Oris Industrie, S.A.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 2
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K881323 | CURIETRON 192 LOW DOSE RATE | January 17, 1989 |
| K860311 | ACTHK-PR RIA KIT | April 7, 1986 |