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MICROLIFE WRIST WATCH BLOOD PRESSURE MONITOR, MODEL BP-3BU1

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K001182
510(k) Type
Traditional
Applicant
MICROLIFE CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/1/2000
Days to Decision
112 days
Submission Type
Summary

MICROLIFE WRIST WATCH BLOOD PRESSURE MONITOR, MODEL BP-3BU1

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K001182
510(k) Type
Traditional
Applicant
MICROLIFE CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/1/2000
Days to Decision
112 days
Submission Type
Summary