The following data is part of a premarket notification filed by Roche Diagnostics Corp. with the FDA for Cobas Integra Ceruloplasmin.
| Device ID | K062379 |
| 510k Number | K062379 |
| Device Name: | COBAS INTEGRA CERULOPLASMIN |
| Classification | Multi-analyte Controls, All Kinds (assayed) |
| Applicant | ROCHE DIAGNOSTICS CORP. 9115 HAGUE RD. Indianapolis, IN 46250 |
| Contact | Corina Harper |
| Correspondent | Corina Harper ROCHE DIAGNOSTICS CORP. 9115 HAGUE RD. Indianapolis, IN 46250 |
| Product Code | JJY |
| CFR Regulation Number | 862.1660 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2006-08-15 |
| Decision Date | 2007-01-31 |
| Summary: | summary |