The following data is part of a premarket notification filed by Roche Diagnostics Corp. with the FDA for Accu-chek 360 Diabetes Management System.
| Device ID | K080227 |
| 510k Number | K080227 |
| Device Name: | ACCU-CHEK 360 DIABETES MANAGEMENT SYSTEM |
| Classification | Accessories, Pump, Infusion |
| Applicant | ROCHE DIAGNOSTICS CORP. 9115 HAGUE RD. Indianapolis, IN 46250 |
| Contact | Scott Thiel |
| Correspondent | Scott Thiel ROCHE DIAGNOSTICS CORP. 9115 HAGUE RD. Indianapolis, IN 46250 |
| Product Code | MRZ |
| CFR Regulation Number | 880.5725 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Abbreviated |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2008-01-30 |
| Decision Date | 2008-05-15 |
| Summary: | summary |