Joytech Healthcare Co. , Ltd. · Class II · Cleared Nov 22, 2017
| K-number | K170666 |
| Device name | The Wrist-Type Fully Automatic Digital Blood Pressure Monitors |
| Applicant | Joytech Healthcare Co. , Ltd. |
| Product code | DXN |
| Device class | Class II |
| Decision date | Nov 22, 2017 |
| 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