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FDA 510(k)

SMITHWICK CAROTID SHUNT

K-Number: K021608 · 2002-10-22

ApplicantImplantable Devices
Decision Date2002-10-22
Product CodeDXC
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

SMITHWICK CAROTID SHUNT is the device name listed in this FDA 510(k) record. The listed applicant is Implantable Devices. It received FDA 510(k) clearance on 2002-10-22 under 510(k) number K021608. The device is classified under product code DXC. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SMITHWICK CAROTID SHUNT?

SMITHWICK CAROTID SHUNT is a medical device that received FDA 510(k) clearance on 2002-10-22. The listed applicant is Implantable Devices. The 510(k) number is K021608.

When did SMITHWICK CAROTID SHUNT receive FDA 510(k) clearance?

SMITHWICK CAROTID SHUNT received FDA 510(k) clearance on 2002-10-22, under 510(k) number K021608.

Who is the listed applicant for SMITHWICK CAROTID SHUNT?

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

What is the FDA product code for SMITHWICK CAROTID SHUNT?

The FDA product code for SMITHWICK CAROTID SHUNT is DXC.

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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.

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