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Upper Arm Blood Pressure Monitor

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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