Rossmax International , Ltd. · Class II · Cleared Jan 17, 2002
| K-number | K013539 |
| Device name | ROSSMAX MEDIPRO, MODELS 100F, 200F, AND 300F BLOOD PRESSURE MONITORS |
| Applicant | Rossmax International , Ltd. |
| Product code | DXN |
| Device class | Class II |
| Decision date | Jan 17, 2002 |
| Decision | Substantially Equivalent |
| Regulation | 870.1130 |
AI extraction for this record is queued and will appear within 24 hours. View full FDA record →
View the full FDA submission: accessdata.fda.gov