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SpyGlass Discover Balloon Dilation Catheter

Page Type
Cleared 510(K)
510(k) Number
K212582
510(k) Type
Traditional
Applicant
Boston Scientific Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/6/2022
Days to Decision
263 days
Submission Type
Summary

SpyGlass Discover Balloon Dilation Catheter

Page Type
Cleared 510(K)
510(k) Number
K212582
510(k) Type
Traditional
Applicant
Boston Scientific Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/6/2022
Days to Decision
263 days
Submission Type
Summary