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VersaCross Steerable Sheath, VersaCross Transseptal Dilator

Page Type
Cleared 510(K)
510(k) Number
K190688
510(k) Type
Special
Applicant
Baylis Medical Company, Inc.
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
4/17/2019
Days to Decision
30 days
Submission Type
Summary

VersaCross Steerable Sheath, VersaCross Transseptal Dilator

Page Type
Cleared 510(K)
510(k) Number
K190688
510(k) Type
Special
Applicant
Baylis Medical Company, Inc.
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
4/17/2019
Days to Decision
30 days
Submission Type
Summary