510(k) K220414

Device
VersaCross Connect Transseptal Dilator
Applicant
Baylis Medical Company, Inc.
510(k) number
K220414
Product code
DYB
Decision
Substantially Equivalent (SESE)
Decision date
2022-05-09
Date received
2022-02-14
Regulation
870.1340
Classification name
Introducer, Catheter
Medical specialty
Cardiovascular
Review panel
Cardiovascular
Device class
2
Clearance type
Special
Statement or summary
Summary
Third party reviewed
No

Applicant Contact#

Contact
May Tsai
Address
5825 Explorer Dr. Mississauga CA L4W 5P6 L4W 5P6

FDA Registration Numbers#

Source Documents#

510(k) summary PDF

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