FDA 510(k)

Electroporation System (N3000)

Número K: K240376 · 2024-10-04

RequerenteSurgnova Healthcare Technologies (Zhejiang) Co., Ltd.

Data da decisão2024-10-04

Código do produtoOAB

Comité consultivoSU

DecisãoSubstantially Equivalent

Resumo do dispositivo

Electroporation System (N3000) is the device name listed in this FDA 510(k) record. The listed applicant is Surgnova Healthcare Technologies (Zhejiang) Co., Ltd.. It received FDA 510(k) clearance on 2024-10-04 under 510(k) number K240376. The device is classified under product code OAB. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the Electroporation System (N3000)?

Electroporation System (N3000) is a medical device that received FDA 510(k) clearance on 2024-10-04. The listed applicant is Surgnova Healthcare Technologies (Zhejiang) Co., Ltd.. The 510(k) number is K240376.

When did Electroporation System (N3000) receive FDA 510(k) clearance?

Electroporation System (N3000) received FDA 510(k) clearance on 2024-10-04, under 510(k) number K240376.

Who is the listed applicant for Electroporation System (N3000)?

The FDA 510(k) record lists Surgnova Healthcare Technologies (Zhejiang) Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Electroporation System (N3000)?

The FDA product code for Electroporation System (N3000) is OAB.

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Fonte oficial

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