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VersaCross Transseptal Sheath

Page Type
Cleared 510(K)
510(k) Number
K183655
510(k) Type
Traditional
Applicant
Baylis Medical Company Inc.
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
5/20/2019
Days to Decision
144 days
Submission Type
Summary

VersaCross Transseptal Sheath

Page Type
Cleared 510(K)
510(k) Number
K183655
510(k) Type
Traditional
Applicant
Baylis Medical Company Inc.
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
5/20/2019
Days to Decision
144 days
Submission Type
Summary