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Scepter Mini Occlusion Balloon Catheter

Page Type
Cleared 510(K)
510(k) Number
K182829
510(k) Type
Traditional
Applicant
MicroVention Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/10/2019
Days to Decision
278 days
Submission Type
Summary

Scepter Mini Occlusion Balloon Catheter

Page Type
Cleared 510(K)
510(k) Number
K182829
510(k) Type
Traditional
Applicant
MicroVention Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/10/2019
Days to Decision
278 days
Submission Type
Summary