FDA 510(k)

VASOVIEW 6 HARVESTING CANNULA, MODELS VH-2000, VH-2001 & VH-2002

K-Number: K022718 · 2002-08-28

ApplicantGuidant Corporation, Cardiac Surgery

Decision Date2002-08-28

Product CodeGEI

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

VASOVIEW 6 HARVESTING CANNULA, MODELS VH-2000, VH-2001 & VH-2002 is the device name listed in this FDA 510(k) record. The listed applicant is Guidant Corporation, Cardiac Surgery. It received FDA 510(k) clearance on 2002-08-28 under 510(k) number K022718. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VASOVIEW 6 HARVESTING CANNULA, MODELS VH-2000, VH-2001 & VH-2002?

VASOVIEW 6 HARVESTING CANNULA, MODELS VH-2000, VH-2001 & VH-2002 is a medical device that received FDA 510(k) clearance on 2002-08-28. The listed applicant is Guidant Corporation, Cardiac Surgery. The 510(k) number is K022718.

When did VASOVIEW 6 HARVESTING CANNULA, MODELS VH-2000, VH-2001 & VH-2002 receive FDA 510(k) clearance?

VASOVIEW 6 HARVESTING CANNULA, MODELS VH-2000, VH-2001 & VH-2002 received FDA 510(k) clearance on 2002-08-28, under 510(k) number K022718.

Who is the listed applicant for VASOVIEW 6 HARVESTING CANNULA, MODELS VH-2000, VH-2001 & VH-2002?

The FDA 510(k) record lists Guidant Corporation, Cardiac Surgery as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VASOVIEW 6 HARVESTING CANNULA, MODELS VH-2000, VH-2001 & VH-2002?

The FDA product code for VASOVIEW 6 HARVESTING CANNULA, MODELS VH-2000, VH-2001 & VH-2002 is GEI.

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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.