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FDA 510(k)

INTERVASCULAR INTERGARD KNITTED VASCULAR GRAFT SIZER

K-Number: K022242 · 2002-08-14

ApplicantIntervascular
Decision Date2002-08-14
Product CodeDSY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

INTERVASCULAR INTERGARD KNITTED VASCULAR GRAFT SIZER is the device name listed in this FDA 510(k) record. The listed applicant is Intervascular. It received FDA 510(k) clearance on 2002-08-14 under 510(k) number K022242. The device is classified under product code DSY. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INTERVASCULAR INTERGARD KNITTED VASCULAR GRAFT SIZER?

INTERVASCULAR INTERGARD KNITTED VASCULAR GRAFT SIZER is a medical device that received FDA 510(k) clearance on 2002-08-14. The listed applicant is Intervascular. The 510(k) number is K022242.

When did INTERVASCULAR INTERGARD KNITTED VASCULAR GRAFT SIZER receive FDA 510(k) clearance?

INTERVASCULAR INTERGARD KNITTED VASCULAR GRAFT SIZER received FDA 510(k) clearance on 2002-08-14, under 510(k) number K022242.

Who is the listed applicant for INTERVASCULAR INTERGARD KNITTED VASCULAR GRAFT SIZER?

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

What is the FDA product code for INTERVASCULAR INTERGARD KNITTED VASCULAR GRAFT SIZER?

The FDA product code for INTERVASCULAR INTERGARD KNITTED VASCULAR GRAFT SIZER is DSY.

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Other records listing Intervascular 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.

K042984INTERGARD WOVEN CONNECTOR GRAFT, MODEL IGW0030-10CK013651INTERGARD HEMABRIDGE COLLAGEN COATED VASCULAR PROSTHESIS, INTERGARD AORTIC ARCH COLLAGEN COATED VASCULAR PROSTHESIS

Related Devices (Code: DSY)

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.

K252445Fusion Bioline Vascular GraftMaquet Cardiovascular, LLCK252277Spiral Laminar Flow™ Vascular Arteriovenous Graft (AV0645)Vascular Flow Technologies LimitedK241550Gelweave™ Vascular ProsthesesVascutek, Ltd.K241070Gelsoft™ Plus Vascular ProsthesesVascutek, Ltd.K231972Advanta VXT Vascular Graft, Flixene Vascular GraftAtrium Medical CorporationK240083GORE® PROPATEN® Vascular GraftW. L. Gore & Associates, Inc.

Official Source

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

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