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FDA 510(k)

VASOVIEW 5 HARVESTING CANNULA

K-Number: K020143 · 2002-02-20

ApplicantGuidant Corporation, Cardiac Surgery
Decision Date2002-02-20
Product CodeHET
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

VASOVIEW 5 HARVESTING CANNULA 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 2002-02-20 under 510(k) number K020143. The device is classified under product code HET. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VASOVIEW 5 HARVESTING CANNULA?

VASOVIEW 5 HARVESTING CANNULA is a medical device that received FDA 510(k) clearance on 2002-02-20. The listed applicant is Guidant Corporation, Cardiac Surgery. The 510(k) number is K020143.

When did VASOVIEW 5 HARVESTING CANNULA receive FDA 510(k) clearance?

VASOVIEW 5 HARVESTING CANNULA received FDA 510(k) clearance on 2002-02-20, under 510(k) number K020143.

Who is the listed applicant for VASOVIEW 5 HARVESTING CANNULA?

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 5 HARVESTING CANNULA?

The FDA product code for VASOVIEW 5 HARVESTING CANNULA is HET.

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Other records listing Guidant Corporation, Cardiac Surgery 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.

K080169HEARTSTRING III PROXIMAL SEAL SYSTEMK041340GUIDANT MICROWAVE ABLATION SYSTEMK023630ESSEX ASPIRATION/IRRIGATION INSTRUMENT WITH POSITIONING GUIDE, MODEL SY-1400K024071GUIDANT SYNCRUS INTERNAL CARDIOVERSION SYSTEMK023629ESSEX DISSECTION CANNULA, MODEL SXD-1100, ESSEX DISSECTION TIP, MODEL SXD-1200K022718VASOVIEW 6 HARVESTING CANNULA, MODELS VH-2000, VH-2001 & VH-2002

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Related Devices (Code: HET)

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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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