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FDA 510(k)

HANCOCK VASCULAR GRAFT

K-Number: K820600 · 1982-07-08

ApplicantExtracorporeal Medical Specialities, Inc.
Decision Date1982-07-08
Product CodeDSY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

HANCOCK VASCULAR GRAFT is the device name listed in this FDA 510(k) record. The listed applicant is Extracorporeal Medical Specialities, Inc.. It received FDA 510(k) clearance on 1982-07-08 under 510(k) number K820600. 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 HANCOCK VASCULAR GRAFT?

HANCOCK VASCULAR GRAFT is a medical device that received FDA 510(k) clearance on 1982-07-08. The listed applicant is Extracorporeal Medical Specialities, Inc.. The 510(k) number is K820600.

When did HANCOCK VASCULAR GRAFT receive FDA 510(k) clearance?

HANCOCK VASCULAR GRAFT received FDA 510(k) clearance on 1982-07-08, under 510(k) number K820600.

Who is the listed applicant for HANCOCK VASCULAR GRAFT?

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

What is the FDA product code for HANCOCK VASCULAR GRAFT?

The FDA product code for HANCOCK VASCULAR GRAFT is DSY.

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Other records listing Extracorporeal Medical Specialities, 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.

K843955EXTRACORPOREAL MAXIMA HOLLOW FIBER OXYGENATORK840262HANCOCK PERICARDIAL PATCHK840532HEMOPERFUSION SYSTEM TP-400K840057EXP* 500 PARALLEL PLATE DIALYZERK840146EXP* 700 PARALLEL PLATE DIALYZERK832547ULTRAFILTRATION CONTROLLER

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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

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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