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FDA 510(k)

MODIFIED CAROTID SHUNT W/SPRING REINFORCED LUMEN

K-Number: K872788 · 1987-09-25

ApplicantUresil Corp.
Decision Date1987-09-25
Product CodeDWF
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MODIFIED CAROTID SHUNT W/SPRING REINFORCED LUMEN is the device name listed in this FDA 510(k) record. The listed applicant is Uresil Corp.. It received FDA 510(k) clearance on 1987-09-25 under 510(k) number K872788. 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 MODIFIED CAROTID SHUNT W/SPRING REINFORCED LUMEN?

MODIFIED CAROTID SHUNT W/SPRING REINFORCED LUMEN is a medical device that received FDA 510(k) clearance on 1987-09-25. The listed applicant is Uresil Corp.. The 510(k) number is K872788.

When did MODIFIED CAROTID SHUNT W/SPRING REINFORCED LUMEN receive FDA 510(k) clearance?

MODIFIED CAROTID SHUNT W/SPRING REINFORCED LUMEN received FDA 510(k) clearance on 1987-09-25, under 510(k) number K872788.

Who is the listed applicant for MODIFIED CAROTID SHUNT W/SPRING REINFORCED LUMEN?

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

What is the FDA product code for MODIFIED CAROTID SHUNT W/SPRING REINFORCED LUMEN?

The FDA product code for MODIFIED CAROTID SHUNT W/SPRING REINFORCED LUMEN is 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.

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