Doran Instruments, Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 2
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
| K913239 | GOLDLENS(TM) | January 31, 1992 |
| K863956 | MACULOSCOPE(TM) | November 13, 1986 |