Last synced on 14 November 2025 at 11:06 pm

VersaCross Connect™ Transseptal Dilator

Page Type
Cleared 510(K)
510(k) Number
K251325
510(k) Type
Special
Applicant
Baylis Medical Company Inc.
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
5/29/2025
Days to Decision
30 days
Submission Type
Summary

VersaCross Connect™ Transseptal Dilator

Page Type
Cleared 510(K)
510(k) Number
K251325
510(k) Type
Special
Applicant
Baylis Medical Company Inc.
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
5/29/2025
Days to Decision
30 days
Submission Type
Summary