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Automated ankle brachial pressure index measuring device, MESI mTABLET system

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K201046
510(k) Type
Traditional
Applicant
Mesi D.O.O.; Mesi, Development of medical devices, Ltd.
Country
Slovenia
FDA Decision
Substantially Equivalent
Decision Date
12/11/2020
Days to Decision
234 days
Submission Type
Summary

Automated ankle brachial pressure index measuring device, MESI mTABLET system

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K201046
510(k) Type
Traditional
Applicant
Mesi D.O.O.; Mesi, Development of medical devices, Ltd.
Country
Slovenia
FDA Decision
Substantially Equivalent
Decision Date
12/11/2020
Days to Decision
234 days
Submission Type
Summary