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Instylla Microcatheter

Page Type
Cleared 510(K)
510(k) Number
K191731
510(k) Type
Traditional
Applicant
Instylla, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/13/2019
Days to Decision
46 days
Submission Type
Summary

Instylla Microcatheter

Page Type
Cleared 510(K)
510(k) Number
K191731
510(k) Type
Traditional
Applicant
Instylla, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/13/2019
Days to Decision
46 days
Submission Type
Summary