The following data is part of a premarket notification filed by Hybritech, Inc. with the FDA for Ferritin Kit.
| Device ID | K812597 |
| 510k Number | K812597 |
| Device Name: | FERRITIN KIT |
| Classification | Ferritin, Antigen, Antiserum, Control |
| Applicant | HYBRITECH, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | DBF |
| CFR Regulation Number | 866.5340 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1981-09-14 |
| Decision Date | 1981-10-19 |