Aneroid Sphygmomanometer; Single Patient Use Aneroid Sphygmomanometer— 510(k) K222652
Substantially EquivalentCardicare Company, Ltd.
FDA 510(k) clearance K222652 for Aneroid Sphygmomanometer; Single Patient Use Aneroid Sphygmomanometer, Substantially Equivalent on 2022-11-28. Applicant: Cardicare Company, Ltd..
Clearance details
- Applicant
- Cardicare Company, Ltd.
- Product code
- Code DXQ
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Hangzhou City, CN
Data sourced from openFDA. This site is unofficial and independent of the FDA.