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V8 Transluminal BAV Catheter

Page Type
Cleared 510(K)
510(k) Number
K150343
510(k) Type
Special
Applicant
InterValve, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/3/2015
Days to Decision
51 days
Submission Type
Summary

V8 Transluminal BAV Catheter

Page Type
Cleared 510(K)
510(k) Number
K150343
510(k) Type
Special
Applicant
InterValve, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/3/2015
Days to Decision
51 days
Submission Type
Summary