FDA 510(k)

M3290B Patient Information Center iX

Número K: K183387 · 2019-08-06

Data da decisão2019-08-06

Código do produtoMHX

Comité consultivoCV

DecisãoSubstantially Equivalent

Resumo do dispositivo

M3290B Patient Information Center iX is the device name listed in this FDA 510(k) record. The listed applicant is Philips Medical Systems. It received FDA 510(k) clearance on 2019-08-06 under 510(k) number K183387. The device is classified under product code MHX. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the M3290B Patient Information Center iX?

M3290B Patient Information Center iX is a medical device that received FDA 510(k) clearance on 2019-08-06. The listed applicant is Philips Medical Systems. The 510(k) number is K183387.

When did M3290B Patient Information Center iX receive FDA 510(k) clearance?

M3290B Patient Information Center iX received FDA 510(k) clearance on 2019-08-06, under 510(k) number K183387.

Who is the listed applicant for M3290B Patient Information Center iX?

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

What is the FDA product code for M3290B Patient Information Center iX?

The FDA product code for M3290B Patient Information Center iX is MHX.

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Outros registros que listam Philips Medical Systems como candidato(a)

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Fonte oficial

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