| K-number | K830580 |
| Device name | DIAGNON FERRITIN 125 I RIA KIT |
| Applicant | Iagnon Corp. |
| Product code | DBF |
| Device class | Class II |
| Decision date | May 5, 1983 |
| Decision | Substantially Equivalent |
| Regulation | 866.5340 |
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