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Ventripoint Medical System Plus (VMS+)

Page Type
Cleared 510(K)
510(k) Number
K173810
510(k) Type
Traditional
Applicant
Ventripoint Diagnostics, Ltd.
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
5/14/2018
Days to Decision
150 days
Submission Type
Summary

Ventripoint Medical System Plus (VMS+)

Page Type
Cleared 510(K)
510(k) Number
K173810
510(k) Type
Traditional
Applicant
Ventripoint Diagnostics, Ltd.
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
5/14/2018
Days to Decision
150 days
Submission Type
Summary