FDA 510(k)

X-View 3D Pan/X-View 2D Pan

Número K: K222666 · 2023-07-10

Data da decisão2023-07-10

Código do produtoOAS

Comité consultivoRA

DecisãoSubstantially Equivalent

Resumo do dispositivo

X-View 3D Pan/X-View 2D Pan is the device name listed in this FDA 510(k) record. The listed applicant is Trident S.R.L. It received FDA 510(k) clearance on 2023-07-10 under 510(k) number K222666. The device is classified under product code OAS. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the X-View 3D Pan/X-View 2D Pan?

X-View 3D Pan/X-View 2D Pan is a medical device that received FDA 510(k) clearance on 2023-07-10. The listed applicant is Trident S.R.L. The 510(k) number is K222666.

When did X-View 3D Pan/X-View 2D Pan receive FDA 510(k) clearance?

X-View 3D Pan/X-View 2D Pan received FDA 510(k) clearance on 2023-07-10, under 510(k) number K222666.

Who is the listed applicant for X-View 3D Pan/X-View 2D Pan?

The FDA 510(k) record lists Trident S.R.L as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for X-View 3D Pan/X-View 2D Pan?

The FDA product code for X-View 3D Pan/X-View 2D Pan is OAS.

Outros registros que listam Trident S.R.L como candidato(a)

Registros relacionados são pareados automaticamente usando nomes, códigos de produtos ou outros metadados. Um pareamento não estabelece um vínculo clínico, científico, corporativo ou regulatório verificado; revise as fontes oficiais vinculadas.

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Fonte oficial

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