FDA 510(k)

MS-39

Número K: K221601 · 2023-09-01

Data da decisão2023-09-01

Código do produtoOBO

Comité consultivoOP

DecisãoSubstantially Equivalent

Resumo do dispositivo

MS-39 is the device name listed in this FDA 510(k) record. The listed applicant is C.S.O. S.R.L.. It received FDA 510(k) clearance on 2023-09-01 under 510(k) number K221601. The device is classified under product code OBO. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the MS-39?

MS-39 is a medical device that received FDA 510(k) clearance on 2023-09-01. The listed applicant is C.S.O. S.R.L.. The 510(k) number is K221601.

When did MS-39 receive FDA 510(k) clearance?

MS-39 received FDA 510(k) clearance on 2023-09-01, under 510(k) number K221601.

Who is the listed applicant for MS-39?

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

What is the FDA product code for MS-39?

The FDA product code for MS-39 is OBO.

Dispositivos Relacionados (Código: OBO)

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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