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V8 Balloon Aortic Valvuloplasty Catheter

Page Type
Cleared 510(K)
510(k) Number
K152150
510(k) Type
Traditional
Applicant
InterValve, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/18/2015
Days to Decision
137 days
Submission Type
Summary

V8 Balloon Aortic Valvuloplasty Catheter

Page Type
Cleared 510(K)
510(k) Number
K152150
510(k) Type
Traditional
Applicant
InterValve, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/18/2015
Days to Decision
137 days
Submission Type
Summary