FDA 510(k)

syngo.CT Single Source Dual Energy (Twin Beam)

Número K: K153220 · 2016-02-19

RequerenteSiemens Medical Solutions USA, Inc.

Data da decisão2016-02-19

Código do produtoJAK

Comité consultivoRA

DecisãoSubstantially Equivalent

Resumo do dispositivo

syngo.CT Single Source Dual Energy (Twin Beam) is the device name listed in this FDA 510(k) record. The listed applicant is Siemens Medical Solutions USA, Inc.. It received FDA 510(k) clearance on 2016-02-19 under 510(k) number K153220. The device is classified under product code JAK. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the syngo.CT Single Source Dual Energy (Twin Beam)?

syngo.CT Single Source Dual Energy (Twin Beam) is a medical device that received FDA 510(k) clearance on 2016-02-19. The listed applicant is Siemens Medical Solutions USA, Inc.. The 510(k) number is K153220.

When did syngo.CT Single Source Dual Energy (Twin Beam) receive FDA 510(k) clearance?

syngo.CT Single Source Dual Energy (Twin Beam) received FDA 510(k) clearance on 2016-02-19, under 510(k) number K153220.

Who is the listed applicant for syngo.CT Single Source Dual Energy (Twin Beam)?

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

What is the FDA product code for syngo.CT Single Source Dual Energy (Twin Beam)?

The FDA product code for syngo.CT Single Source Dual Energy (Twin Beam) is JAK.

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Fonte oficial

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