FDA 510(k)

Cios Spin

Número K: K210054 · 2021-02-05

RequerenteSiemens Medical Systems USA, Inc.

Data da decisão2021-02-05

Código do produtoOWB

Comité consultivoRA

DecisãoSubstantially Equivalent

Resumo do dispositivo

Cios Spin is the device name listed in this FDA 510(k) record. The listed applicant is Siemens Medical Systems USA, Inc.. It received FDA 510(k) clearance on 2021-02-05 under 510(k) number K210054. The device is classified under product code OWB. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the Cios Spin?

Cios Spin is a medical device that received FDA 510(k) clearance on 2021-02-05. The listed applicant is Siemens Medical Systems USA, Inc.. The 510(k) number is K210054.

When did Cios Spin receive FDA 510(k) clearance?

Cios Spin received FDA 510(k) clearance on 2021-02-05, under 510(k) number K210054.

Who is the listed applicant for Cios Spin?

The FDA 510(k) record lists Siemens Medical Systems USA, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Cios Spin?

The FDA product code for Cios Spin is OWB.

Outros registros que listam Siemens Medical Systems USA, Inc. 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.

K181560Cios Alpha

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Fonte oficial

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