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FDA 510(k)

GUIDANT VASOVIEW ENDOSCOPIC VESSEL HARVESTING SYSTEM

K-Number: K030512 · 2003-05-14

ApplicantGuidant Corp.
Decision Date2003-05-14
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

GUIDANT VASOVIEW ENDOSCOPIC VESSEL HARVESTING SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Guidant Corp.. It received FDA 510(k) clearance on 2003-05-14 under 510(k) number K030512. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GUIDANT VASOVIEW ENDOSCOPIC VESSEL HARVESTING SYSTEM?

GUIDANT VASOVIEW ENDOSCOPIC VESSEL HARVESTING SYSTEM is a medical device that received FDA 510(k) clearance on 2003-05-14. The listed applicant is Guidant Corp.. The 510(k) number is K030512.

When did GUIDANT VASOVIEW ENDOSCOPIC VESSEL HARVESTING SYSTEM receive FDA 510(k) clearance?

GUIDANT VASOVIEW ENDOSCOPIC VESSEL HARVESTING SYSTEM received FDA 510(k) clearance on 2003-05-14, under 510(k) number K030512.

Who is the listed applicant for GUIDANT VASOVIEW ENDOSCOPIC VESSEL HARVESTING SYSTEM?

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

What is the FDA product code for GUIDANT VASOVIEW ENDOSCOPIC VESSEL HARVESTING SYSTEM?

The FDA product code for GUIDANT VASOVIEW ENDOSCOPIC VESSEL HARVESTING SYSTEM is GCJ.

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Related Devices (Code: GCJ)

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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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