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Upper Arm Blood Pressure Monitor

Page Type
Cleared 510(K)
510(k) Number
K191673
510(k) Type
Traditional
Applicant
Famidoc Technology Company Limited
Country
China
FDA Decision
Substantially Equivalent
Decision Date
11/27/2019
Days to Decision
156 days
Submission Type
Summary

Upper Arm Blood Pressure Monitor

Page Type
Cleared 510(K)
510(k) Number
K191673
510(k) Type
Traditional
Applicant
Famidoc Technology Company Limited
Country
China
FDA Decision
Substantially Equivalent
Decision Date
11/27/2019
Days to Decision
156 days
Submission Type
Summary