The following data is part of a premarket notification filed by Roche Diagnostics Corp. with the FDA for Elecsys Precicontrol Anemia.
| Device ID | K051517 |
| 510k Number | K051517 |
| Device Name: | ELECSYS PRECICONTROL ANEMIA |
| Classification | Multi-analyte Controls, All Kinds (assayed) |
| Applicant | ROCHE DIAGNOSTICS CORP. 9115 HAGUE RD. Indianapolis, IN 46250 |
| Contact | Cornia Harper |
| Correspondent | Cornia 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 | 2005-06-08 |
| Decision Date | 2005-07-05 |
| Summary: | summary |