FDA 510(k)

Lunderquist Extra Stiff Wire Guide

Número K: K171513 · 2017-12-07

Data da decisão2017-12-07

Código do produtoDQX

Comité consultivoCV

DecisãoSubstantially Equivalent

Resumo do dispositivo

Lunderquist Extra Stiff Wire Guide is the device name listed in this FDA 510(k) record. The listed applicant is William Cook Europe Aps. It received FDA 510(k) clearance on 2017-12-07 under 510(k) number K171513. The device is classified under product code DQX. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the Lunderquist Extra Stiff Wire Guide?

Lunderquist Extra Stiff Wire Guide is a medical device that received FDA 510(k) clearance on 2017-12-07. The listed applicant is William Cook Europe Aps. The 510(k) number is K171513.

When did Lunderquist Extra Stiff Wire Guide receive FDA 510(k) clearance?

Lunderquist Extra Stiff Wire Guide received FDA 510(k) clearance on 2017-12-07, under 510(k) number K171513.

Who is the listed applicant for Lunderquist Extra Stiff Wire Guide?

The FDA 510(k) record lists William Cook Europe Aps as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Lunderquist Extra Stiff Wire Guide?

The FDA product code for Lunderquist Extra Stiff Wire Guide is DQX.

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Outros registros que listam William Cook Europe Aps como candidato(a)

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Fonte oficial

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