Kamiya Biomedical Co. · Class II · Cleared Dec 23, 2005
| K-number | K050944 |
| Device name | K-ASSAY FERRITIN (2) & FERRITIN CALIBRATOR SET |
| Applicant | Kamiya Biomedical Co. |
| Product code | DBF |
| Device class | Class II |
| Decision date | Dec 23, 2005 |
| 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