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FDA 510(k)

VersaCross Connect™ Transseptal Dilator

K-Number: K233647 · 2023-12-14

ApplicantBaylis Medical Company, Inc.
Decision Date2023-12-14
Product CodeDRE
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

VersaCross Connect™ Transseptal Dilator is the device name listed in this FDA 510(k) record. The listed applicant is Baylis Medical Company, Inc.. It received FDA 510(k) clearance on 2023-12-14 under 510(k) number K233647. The device is classified under product code DRE. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VersaCross Connect™ Transseptal Dilator?

VersaCross Connect™ Transseptal Dilator is a medical device that received FDA 510(k) clearance on 2023-12-14. The listed applicant is Baylis Medical Company, Inc.. The 510(k) number is K233647.

When did VersaCross Connect™ Transseptal Dilator receive FDA 510(k) clearance?

VersaCross Connect™ Transseptal Dilator received FDA 510(k) clearance on 2023-12-14, under 510(k) number K233647.

Who is the listed applicant for VersaCross Connect™ Transseptal Dilator?

The FDA 510(k) record lists Baylis Medical Company, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VersaCross Connect™ Transseptal Dilator?

The FDA product code for VersaCross Connect™ Transseptal Dilator is DRE.

Other records listing Baylis Medical Company, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K251325VersaCross Connect™ Transseptal DilatorK242076VersaCross™ RF WireK241720VersaCross Connect™ Transseptal DilatorK231227SureFlex HD Steerable Sheath, VersaCross HD Steerable SheathK213898ProTrack Pigtail WireK221351Mechanical Guidewire

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Related Devices (Code: DRE)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K261310FlexTract Deflectable-Rotational Dilator Sheath SetMerit Medical Systems, Inc.K253616ProtekDilate Vascular Access KitSorin Group Italia S.R.L.K251325VersaCross Connect™ Transseptal DilatorBaylis Medical Company, Inc.K242229Micro Ace Gold Advanced Micro Access SystemMerit Medical Systems, Inc.K241720VersaCross Connect™ Transseptal DilatorBaylis Medical Company, Inc.K232609Micro Ace™ Advanced Micro Access SystemMerit Medical Systems, Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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