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087 Balloon Guide Catheter System

Page Type
Cleared 510(K)
510(k) Number
K190749
510(k) Type
Traditional
Applicant
Q'Apel
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/15/2019
Days to Decision
112 days
Submission Type
Summary

087 Balloon Guide Catheter System

Page Type
Cleared 510(K)
510(k) Number
K190749
510(k) Type
Traditional
Applicant
Q'Apel
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/15/2019
Days to Decision
112 days
Submission Type
Summary