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Aneroid Sphygmomanometer; Single Patient Use Aneroid Sphygmomanometer

Page Type
Cleared 510(K)
510(k) Number
K222652
510(k) Type
Traditional
Applicant
Cardicare Company, Ltd.
Country
China
FDA Decision
Substantially Equivalent
Decision Date
11/28/2022
Days to Decision
88 days
Submission Type
Summary

Aneroid Sphygmomanometer; Single Patient Use Aneroid Sphygmomanometer

Page Type
Cleared 510(K)
510(k) Number
K222652
510(k) Type
Traditional
Applicant
Cardicare Company, Ltd.
Country
China
FDA Decision
Substantially Equivalent
Decision Date
11/28/2022
Days to Decision
88 days
Submission Type
Summary