510(k) K241720

Device
VersaCross Connect™ Transseptal Dilator
Applicant
Baylis Medical Company, Inc.
510(k) number
K241720
Product code
DRE
Decision
Substantially Equivalent (SESE)
Decision date
2024-07-12
Date received
2024-06-14
Regulation
870.1310
Classification name
Dilator, Vessel, For Percutaneous Catheterization
Medical specialty
Cardiovascular
Review panel
Cardiovascular
Device class
2
Clearance type
Special
Statement or summary
Summary
Third party reviewed
N
Source
FDA openFDA 510(k) dataset plus migrated FDA.report data

Related Records

Applicant Contact

Contact
Ezgi Tas
Address
5825 Explorer Dr. Mississauga CA L4W5P6 L4W5P6

FDA Registration Numbers

Source Documents

FDA 510(k) Premarket Notification Database · 510(k) summary PDF · openFDA JSON

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K200379Super SheathTogo Medikit Co., Ltd.2020-03-19
K192195Sterile DilatorGalt Medical Corp.2019-09-26
K190175S-MAK XLMerit Medical Systems, Inc.2019-04-10
K182064ExpanSure Transseptal Dilation SystemBaylis Medical Company, Inc.2019-03-21