Cardicare Company, Ltd.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 2
- Inspections
- 1
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K222652 | Aneroid Sphygmomanometer; Single Patient Use Aneroid Sphygmomanometer | November 28, 2022 |
| K082542 | ANEROID SPHYGMOMANOMETER WITH STETHOSCOPE MODEL HBPK-A | September 17, 2008 |