Last synced on 20 December 2024 at 11:05 pm

VenSure™ Balloon Dilation System, VenSure™ Light Balloon Dilation System, VenSure™ Nav Balloon Dilation System, VenSure™ ET Balloon Dilation System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K230065
510(k) Type
Traditional
Applicant
Fiagon GmbH
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
5/26/2023
Days to Decision
137 days
Submission Type
Summary

VenSure™ Balloon Dilation System, VenSure™ Light Balloon Dilation System, VenSure™ Nav Balloon Dilation System, VenSure™ ET Balloon Dilation System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K230065
510(k) Type
Traditional
Applicant
Fiagon GmbH
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
5/26/2023
Days to Decision
137 days
Submission Type
Summary