Last synced on 25 April 2025 at 11:05 pm

VENTRIPOINT MEDICAL SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K140153
510(k) Type
Traditional
Applicant
VENTRIPOINT, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/6/2014
Days to Decision
43 days
Submission Type
Summary

VENTRIPOINT MEDICAL SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K140153
510(k) Type
Traditional
Applicant
VENTRIPOINT, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/6/2014
Days to Decision
43 days
Submission Type
Summary