FDA 510(k)

Microlife Upper Arm Automatic Digital Blood Pressure Monitor

Número K: K190818 · 2019-07-10

RequerenteMicrolife Intellectual Property GmbH

Data da decisão2019-07-10

Código do produtoDXN

Comité consultivoCV

DecisãoSubstantially Equivalent

Resumo do dispositivo

Microlife Upper Arm Automatic Digital Blood Pressure Monitor is the device name listed in this FDA 510(k) record. The listed applicant is Microlife Intellectual Property GmbH. It received FDA 510(k) clearance on 2019-07-10 under 510(k) number K190818. The device is classified under product code DXN. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the Microlife Upper Arm Automatic Digital Blood Pressure Monitor?

Microlife Upper Arm Automatic Digital Blood Pressure Monitor is a medical device that received FDA 510(k) clearance on 2019-07-10. The listed applicant is Microlife Intellectual Property GmbH. The 510(k) number is K190818.

When did Microlife Upper Arm Automatic Digital Blood Pressure Monitor receive FDA 510(k) clearance?

Microlife Upper Arm Automatic Digital Blood Pressure Monitor received FDA 510(k) clearance on 2019-07-10, under 510(k) number K190818.

Who is the listed applicant for Microlife Upper Arm Automatic Digital Blood Pressure Monitor?

The FDA 510(k) record lists Microlife Intellectual Property GmbH as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Microlife Upper Arm Automatic Digital Blood Pressure Monitor?

The FDA product code for Microlife Upper Arm Automatic Digital Blood Pressure Monitor is DXN.

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Outros registros que listam Microlife Intellectual Property GmbH como candidato(a)

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