FDA 510(k)

PATIENT MONITORS VARIOUS MODELS

Número K: K151812 · 2016-01-26

Data da decisão2016-01-26

Código do produtoMHX

Comité consultivoCV

DecisãoSubstantially Equivalent

Resumo do dispositivo

PATIENT MONITORS VARIOUS MODELS 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 2016-01-26 under 510(k) number K151812. 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 PATIENT MONITORS VARIOUS MODELS?

PATIENT MONITORS VARIOUS MODELS is a medical device that received FDA 510(k) clearance on 2016-01-26. The listed applicant is Philips Medical Systems. The 510(k) number is K151812.

When did PATIENT MONITORS VARIOUS MODELS receive FDA 510(k) clearance?

PATIENT MONITORS VARIOUS MODELS received FDA 510(k) clearance on 2016-01-26, under 510(k) number K151812.

Who is the listed applicant for PATIENT MONITORS VARIOUS MODELS?

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 PATIENT MONITORS VARIOUS MODELS?

The FDA product code for PATIENT MONITORS VARIOUS MODELS is MHX.

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

K212704Philips EPIQ Diagnostic Ultrasound System, Philips Affiniti Diagnostic Ultrasound System K211597EPIQ Series Diagnostic Ultrasound System, Affiniti Series Diagnostic Ultrasound System K210560Page Writer TC20 Cardiograph, Page Writer TC30 Cardiograph, Page Writer TC50 Cardiograph, Page Writer TC70 Cardiograph K191738PageWriter TC20 Cardiograph, PageWriter TC30 Cardiograph, PageWriter TC50 Cardiograph, PageWriter TC70 Cardiograph K192875Philips Biosensor BX100 K183387M3290B Patient Information Center iX

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