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FDA 510(k)

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 the device name listed in this FDA 510(k) record. The listed applicant is Cook Incorporated. It received FDA 510(k) clearance on 2024-03-08 under 510(k) 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. The listed applicant is Cook Incorporated. The 510(k) number is K233177.

When did Nest VT Vitrification Device receive FDA 510(k) clearance?

Nest VT Vitrification Device received FDA 510(k) clearance on 2024-03-08, under 510(k) number K233177.

Who is the listed applicant for Nest VT Vitrification Device?

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

What is the FDA product code for Nest VT Vitrification Device?

The FDA product code for Nest VT Vitrification Device is MQK.

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Related Devices (Code: MQK)

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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.

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