FDA 510(k)

Electrosurgical accessory

Número K: K210394 · 2021-05-19

Data da decisão2021-05-19

Código do produtoFAS

Comité consultivoGU

DecisãoSubstantially Equivalent

Resumo do dispositivo

Electrosurgical accessory is the device name listed in this FDA 510(k) record. The listed applicant is Dornier Medtech America, Inc.. It received FDA 510(k) clearance on 2021-05-19 under 510(k) number K210394. The device is classified under product code FAS. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the Electrosurgical accessory?

Electrosurgical accessory is a medical device that received FDA 510(k) clearance on 2021-05-19. The listed applicant is Dornier Medtech America, Inc.. The 510(k) number is K210394.

When did Electrosurgical accessory receive FDA 510(k) clearance?

Electrosurgical accessory received FDA 510(k) clearance on 2021-05-19, under 510(k) number K210394.

Who is the listed applicant for Electrosurgical accessory?

The FDA 510(k) record lists Dornier Medtech America, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Electrosurgical accessory?

The FDA product code for Electrosurgical accessory is FAS.

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Fonte oficial

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