Nester Embolization Coils, Tornado Embolization Coils
K-Number: K153778 · 2016-05-19
ApplicantCook Incorporated
Decision Date2016-05-19
Product CodeKRD
Advisory CommitteeCV
DecisionSubstantially Equivalent
Device Summary
Nester Embolization Coils, Tornado Embolization Coils is a medical device manufactured by Cook Incorporated. It received FDA 510(k) clearance on 2016-05-19 under approval number K153778. The device is classified under product code KRD. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Nester Embolization Coils, Tornado Embolization Coils?
Nester Embolization Coils, Tornado Embolization Coils is a medical device that received FDA 510(k) clearance on 2016-05-19. It is manufactured by Cook Incorporated. The 510(k) number is K153778.
When was Nester Embolization Coils, Tornado Embolization Coils approved by the FDA?
Nester Embolization Coils, Tornado Embolization Coils received FDA 510(k) clearance on 2016-05-19, under approval number K153778.
What company makes Nester Embolization Coils, Tornado Embolization Coils?
Nester Embolization Coils, Tornado Embolization Coils is manufactured by Cook Incorporated.
What is the FDA product code for Nester Embolization Coils, Tornado Embolization Coils?
The FDA product code for Nester Embolization Coils, Tornado Embolization Coils is KRD.
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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.