Nest VT Vitrification Device
K-Number: K233177 · 2024-03-08
ApplicantCook Incorporated
Decision Date2024-03-08
Product CodeMQK
Advisory CommitteeOB
DecisionSubstantially Equivalent
Device Summary
Nest VT Vitrification Device is a medical device manufactured by Cook Incorporated. It received FDA 510(k) clearance on 2024-03-08 under approval number K233177. The device is classified under product code MQK. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Nest VT Vitrification Device?
Nest VT Vitrification Device is a medical device that received FDA 510(k) clearance on 2024-03-08. It is manufactured by Cook Incorporated. The 510(k) number is K233177.
When was Nest VT Vitrification Device approved by the FDA?
Nest VT Vitrification Device received FDA 510(k) clearance on 2024-03-08, under approval number K233177.
What company makes Nest VT Vitrification Device?
Nest VT Vitrification Device is manufactured by Cook Incorporated.
What is the FDA product code for Nest VT Vitrification Device?
The FDA product code for Nest VT Vitrification Device is MQK.
Related Clinical Trials
Other Devices by Cook Incorporated
Related Devices (Code: MQK)
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.