Rodenstock Instrument 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 |
|---|
| K882517 | RODENSTOCK SCANNING LASER OPHTHALMOSCOPE | January 24, 1989 |
| K781440 | LENSOMETER MODEL 11 | September 7, 1978 |