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MICROLIFE UPPER ARM AUTOMATIC DIGITAL BLOOD PRESSURE MONITOR, MODEL WATCHBP O3

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K082881
510(k) Type
Traditional
Applicant
Microlife Intellectual Property GmbH
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/24/2008
Days to Decision
56 days
Submission Type
Summary

MICROLIFE UPPER ARM AUTOMATIC DIGITAL BLOOD PRESSURE MONITOR, MODEL WATCHBP O3

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K082881
510(k) Type
Traditional
Applicant
Microlife Intellectual Property GmbH
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/24/2008
Days to Decision
56 days
Submission Type
Summary