| K-number | K924186 |
| Device name | LPIA-FERRITIN ASSAY |
| Applicant | Seradyn, Inc. |
| Product code | DEF |
| Device class | Class I |
| Decision date | Dec 23, 1992 |
| Decision | Substantially Equivalent |
| Regulation | 866.5425 |
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