Midwest Eye Laboratories, Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 2
- Inspections
- 3
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K904962 | EYE ARTIFICIAL CUSTOM | August 30, 1991 |
| K904961 | ARTIFICIAL SCLERAL SHELL | August 30, 1991 |