Laser Center Dev. Corp.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 2
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K981235 | OCULOSTAT | July 15, 1998 |
| K981063 | AUTOMATED CORNEAL TREPHINE | June 23, 1998 |