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VenSure Balloon Device, VenSure Nav Balloon Device

Page Type
Cleared 510(K)
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)
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