Cardicare Company, Ltd. · Class II · Cleared Nov 28, 2022
| K-number | K222652 |
| Device name | Aneroid Sphygmomanometer; Single Patient Use Aneroid Sphygmomanometer |
| Applicant | Cardicare Company, Ltd. |
| Product code | DXQ |
| Device class | Class II |
| Decision date | Nov 28, 2022 |
| Decision | Substantially Equivalent |
| Regulation | 870.1120 |
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