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FDA 510(k)

VYGON SPLIT CANNULA INTRODUCER

K-Number: K010913 · 2001-09-28

ApplicantVygon Corp.
Decision Date2001-09-28
Product CodeDYB
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

VYGON SPLIT CANNULA INTRODUCER is the device name listed in this FDA 510(k) record. The listed applicant is Vygon Corp.. It received FDA 510(k) clearance on 2001-09-28 under 510(k) number K010913. 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 VYGON SPLIT CANNULA INTRODUCER?

VYGON SPLIT CANNULA INTRODUCER is a medical device that received FDA 510(k) clearance on 2001-09-28. The listed applicant is Vygon Corp.. The 510(k) number is K010913.

When did VYGON SPLIT CANNULA INTRODUCER receive FDA 510(k) clearance?

VYGON SPLIT CANNULA INTRODUCER received FDA 510(k) clearance on 2001-09-28, under 510(k) number K010913.

Who is the listed applicant for VYGON SPLIT CANNULA INTRODUCER?

The FDA 510(k) record lists Vygon Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VYGON SPLIT CANNULA INTRODUCER?

The FDA product code for VYGON SPLIT CANNULA INTRODUCER is DYB.

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Other records listing Vygon Corp. as applicant

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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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