Double Flexible Tipped Wire Guides
K-Number: K181351 · 2018-06-14
ApplicantCook Incorporated
Decision Date2018-06-14
Product CodeDQX
Advisory CommitteeCV
DecisionSubstantially Equivalent
Device Summary
Double Flexible Tipped Wire Guides is a medical device manufactured by Cook Incorporated. It received FDA 510(k) clearance on 2018-06-14 under approval number K181351. 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 Double Flexible Tipped Wire Guides?
Double Flexible Tipped Wire Guides is a medical device that received FDA 510(k) clearance on 2018-06-14. It is manufactured by Cook Incorporated. The 510(k) number is K181351.
When was Double Flexible Tipped Wire Guides approved by the FDA?
Double Flexible Tipped Wire Guides received FDA 510(k) clearance on 2018-06-14, under approval number K181351.
What company makes Double Flexible Tipped Wire Guides?
Double Flexible Tipped Wire Guides is manufactured by Cook Incorporated.
What is the FDA product code for Double Flexible Tipped Wire Guides?
The FDA product code for Double Flexible Tipped Wire Guides 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.