FDA 510(k)

Nest VT Vitrification Device

Número K: K233177 · 2024-03-08

Data da decisão2024-03-08

Código do produtoMQK

Comité consultivoOB

DecisãoSubstantially Equivalent

Resumo do dispositivo

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.

Perguntas frequentes

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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Fonte oficial

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