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MICROLIFE UPPER ARM MANUAL BLOOD PRESSURE MONITOR, MODEL BP3MR1-H (BP A50)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K073397
510(k) Type
Special
Applicant
MICROLIFE CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/20/2007
Days to Decision
17 days
Submission Type
Summary

MICROLIFE UPPER ARM MANUAL BLOOD PRESSURE MONITOR, MODEL BP3MR1-H (BP A50)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K073397
510(k) Type
Special
Applicant
MICROLIFE CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/20/2007
Days to Decision
17 days
Submission Type
Summary