Last synced on 19 July 2024 at 11:05 pm

VenSure Balloon Device, VenSure Nav Balloon Device

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K201472
510(k) Type
Traditional
Applicant
Fiagon GmbH
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
8/26/2020
Days to Decision
84 days
Submission Type
Summary

VenSure Balloon Device, VenSure Nav Balloon Device

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K201472
510(k) Type
Traditional
Applicant
Fiagon GmbH
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
8/26/2020
Days to Decision
84 days
Submission Type
Summary