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.. Device class: 2.
Clearance details
- Applicant
- Cardicare Company, Ltd.
- Product code
- Code DXQ
- Device class
- Class 2
- Regulation
- 21 CFR 870.1120
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Hangzhou City, CN
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More clearances from Cardicare Company, Ltd.
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