| K-number | K100538 |
| Device name | TINA-QUANT FERRITIN GEN. 4 |
| Applicant | Roche Diagnostics |
| Product code | DBF |
| Device class | Class II |
| Decision date | Jun 22, 2010 |
| Decision | Substantially Equivalent |
| Regulation | 866.5340 |
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