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VersaCross Connect™ Transseptal Dilator

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K233647
510(k) Type
Special
Applicant
Baylis Medical Company Inc.
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
12/14/2023
Days to Decision
30 days
Submission Type
Summary

VersaCross Connect™ Transseptal Dilator

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K233647
510(k) Type
Special
Applicant
Baylis Medical Company Inc.
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
12/14/2023
Days to Decision
30 days
Submission Type
Summary