FDA 510(k)

MEDTRONIC AORTOCORONARY SHUNT AND SEPARATELY PACKAGED ARTERIOTOMY CANNULAE

K-Number: K994171 · 2000-04-27

ApplicantMedtronic Cardiac Surgical Products

Decision Date2000-04-27

Product CodeDWF

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

MEDTRONIC AORTOCORONARY SHUNT AND SEPARATELY PACKAGED ARTERIOTOMY CANNULAE is the device name listed in this FDA 510(k) record. The listed applicant is Medtronic Cardiac Surgical Products. It received FDA 510(k) clearance on 2000-04-27 under 510(k) number K994171. The device is classified under product code DWF. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDTRONIC AORTOCORONARY SHUNT AND SEPARATELY PACKAGED ARTERIOTOMY CANNULAE?

MEDTRONIC AORTOCORONARY SHUNT AND SEPARATELY PACKAGED ARTERIOTOMY CANNULAE is a medical device that received FDA 510(k) clearance on 2000-04-27. The listed applicant is Medtronic Cardiac Surgical Products. The 510(k) number is K994171.

When did MEDTRONIC AORTOCORONARY SHUNT AND SEPARATELY PACKAGED ARTERIOTOMY CANNULAE receive FDA 510(k) clearance?

MEDTRONIC AORTOCORONARY SHUNT AND SEPARATELY PACKAGED ARTERIOTOMY CANNULAE received FDA 510(k) clearance on 2000-04-27, under 510(k) number K994171.

Who is the listed applicant for MEDTRONIC AORTOCORONARY SHUNT AND SEPARATELY PACKAGED ARTERIOTOMY CANNULAE?

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

What is the FDA product code for MEDTRONIC AORTOCORONARY SHUNT AND SEPARATELY PACKAGED ARTERIOTOMY CANNULAE?

The FDA product code for MEDTRONIC AORTOCORONARY SHUNT AND SEPARATELY PACKAGED ARTERIOTOMY CANNULAE is DWF.

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Other records listing Medtronic Cardiac Surgical Products as applicant

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Related Devices (Code: DWF)

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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.