The following data is part of a premarket notification filed by Roche Diagnostics Corp. with the FDA for Ferritin Generation 2.
| Device ID | K031650 |
| 510k Number | K031650 |
| Device Name: | FERRITIN GENERATION 2 |
| Classification | Ferritin, Antigen, Antiserum, Control |
| Applicant | ROCHE DIAGNOSTICS CORP. 9115 HAGUE RD. Indianapolis, IN 46250 |
| Contact | Kay A Taylor |
| Correspondent | Kay A Taylor ROCHE DIAGNOSTICS CORP. 9115 HAGUE RD. Indianapolis, IN 46250 |
| Product Code | DBF |
| CFR Regulation Number | 866.5340 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2003-05-28 |
| Decision Date | 2003-07-17 |
| Summary: | summary |