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FDA 510(k)

TSP Crosser Transseptal Access System

K-Number: K181088 · 2018-09-28

ApplicantTransseptal Solutions , Ltd.
Decision Date2018-09-28
Product CodeDYB
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

TSP Crosser Transseptal Access System is the device name listed in this FDA 510(k) record. The listed applicant is Transseptal Solutions , Ltd.. It received FDA 510(k) clearance on 2018-09-28 under 510(k) number K181088. The device is classified under product code DYB. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TSP Crosser Transseptal Access System?

TSP Crosser Transseptal Access System is a medical device that received FDA 510(k) clearance on 2018-09-28. The listed applicant is Transseptal Solutions , Ltd.. The 510(k) number is K181088.

When did TSP Crosser Transseptal Access System receive FDA 510(k) clearance?

TSP Crosser Transseptal Access System received FDA 510(k) clearance on 2018-09-28, under 510(k) number K181088.

Who is the listed applicant for TSP Crosser Transseptal Access System?

The FDA 510(k) record lists Transseptal Solutions , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TSP Crosser Transseptal Access System?

The FDA product code for TSP Crosser Transseptal Access System is DYB.

Related Clinical Trials

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.

NCT07361445Agilis RF TSP Early Feasibility StudyRECRUITINGNCT07515040Comparative Study on the Safety and Efficacy of Using AccuSafe Transseptal Guidewire Versus Traditional Transseptal Needle for Transseptal Puncture in non-or Free- GuidanceRECRUITING

Related Devices (Code: DYB)

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.

K253526NAMIC Dilator and SheathMedline Industries, LPK261529Micropuncture Kit / Micropuncture Access Kit / Micropuncture Introducer Set/ Microintroducer Kit / Microintroducer Kit (SIS05C); Micropuncture Kit / Micropuncture Access Kit / Micropuncture Introducer Set / Microintroducer Kit / Microintroducer Kit (IS01); Introducer Kit / Microintroducer Kit / Introducer Set /Microintroducer Set / Micro Introducer Sheath Set / Introducer Sheath Set (NIS04)Hartman Medical Group, LLCK261242SimplGuidePendracareK261950Health Line Tearaway IntroducerHealth Line International CorporationK261492FieldFlex Steerable SheathCenterPoint Systems, LLCK260606Echo Large Bore Introducer SheathEcho Medical, LLC

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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