Last synced on 25 April 2025 at 11:05 pm

Ventripoint Medical System Plus (VMS+)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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