Lunderquist Extra Stiff Wire Guide
K-Number: K171513 · 2017-12-07
ApplicantWilliam Cook Europe Aps
Decision Date2017-12-07
Product CodeDQX
Advisory CommitteeCV
DecisionSubstantially Equivalent
Device Summary
Lunderquist Extra Stiff Wire Guide is a medical device manufactured by William Cook Europe Aps. It received FDA 510(k) clearance on 2017-12-07 under approval number K171513. The device is classified under product code DQX. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
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. It is manufactured by William Cook Europe Aps. The 510(k) number is K171513.
When was Lunderquist Extra Stiff Wire Guide approved by the FDA?
Lunderquist Extra Stiff Wire Guide received FDA 510(k) clearance on 2017-12-07, under approval number K171513.
What company makes Lunderquist Extra Stiff Wire Guide?
Lunderquist Extra Stiff Wire Guide is manufactured by William Cook Europe Aps.
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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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.