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MICROLIFE UPPER ARM AUTOMATIC DIGITAL BLOOD PRESSURE MONITOR, CARDIO+ (BP4GAPO-2M)

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K122013
510(k) Type
Traditional
Applicant
Microlife Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/13/2013
Days to Decision
307 days
Submission Type
Summary

MICROLIFE UPPER ARM AUTOMATIC DIGITAL BLOOD PRESSURE MONITOR, CARDIO+ (BP4GAPO-2M)

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K122013
510(k) Type
Traditional
Applicant
Microlife Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/13/2013
Days to Decision
307 days
Submission Type
Summary