Magna Fortis Corporation · Class II · Cleared Sep 12, 2000
| K-number | K002044 |
| Device name | MAGNA FORTIS OPHTHALMOSCOPE DIAGNOSTIC KIT |
| Applicant | Magna Fortis Corporation |
| Product code | HLJ |
| Device class | Class II |
| Decision date | Sep 12, 2000 |
| Decision | Substantially Equivalent |
| Regulation | 886.1570 |
AI extraction for this record is queued and will appear within 24 hours. View full FDA record →
View the full FDA submission: accessdata.fda.gov