Luneau Ophtalmologie SA
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 3
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K922253 | KERATOREF L60 | June 19, 1992 |
| K921214 | OPHTHALMIC PROJECTOR | June 11, 1992 |
| K913961 | OPHTHALMIC STAND | December 4, 1991 |