Class Class II

VersaCross Connect™ Transseptal Dilator (K241720)

K241720 2024-07-12 Special
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Description

VersaCross Connect™ Transseptal Dilator by Baylis Medical Company, Inc. — FDA 510(k) cleared cardiovascular device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK241720
Clearance Date2024-07-12
Clearance TypeSpecial
Product CodeDRE
Regulation Number870.1310

Categories

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