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Microlife Upper Arm Automatic Digital Blood Pressure Monitor

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K151869
510(k) Type
Traditional
Applicant
MICROLIFE INTELLECTUAL PROPERTY GMBH, SWITZERLAND
Country
Switzerland
FDA Decision
Substantially Equivalent
Decision Date
9/2/2015
Days to Decision
55 days
Submission Type
Summary

Microlife Upper Arm Automatic Digital Blood Pressure Monitor

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K151869
510(k) Type
Traditional
Applicant
MICROLIFE INTELLECTUAL PROPERTY GMBH, SWITZERLAND
Country
Switzerland
FDA Decision
Substantially Equivalent
Decision Date
9/2/2015
Days to Decision
55 days
Submission Type
Summary