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FDA 510(k)

RH non-Automated Blood Pressure Meter RH non-Automated Blood Pressure Meter with Stethoscope

Número K: K190902 · 2019-05-22

RequerenteWenzhou Renhua Instruments Co., Ltd.
Data da decisão2019-05-22
Código do produtoDXQ
Comité consultivoCV
DecisãoSubstantially Equivalent

Resumo do dispositivo

RH non-Automated Blood Pressure Meter RH non-Automated Blood Pressure Meter with Stethoscope is the device name listed in this FDA 510(k) record. The listed applicant is Wenzhou Renhua Instruments Co., Ltd.. It received FDA 510(k) clearance on 2019-05-22 under 510(k) number K190902. The device is classified under product code DXQ. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the RH non-Automated Blood Pressure Meter RH non-Automated Blood Pressure Meter with Stethoscope?

RH non-Automated Blood Pressure Meter RH non-Automated Blood Pressure Meter with Stethoscope is a medical device that received FDA 510(k) clearance on 2019-05-22. The listed applicant is Wenzhou Renhua Instruments Co., Ltd.. The 510(k) number is K190902.

When did RH non-Automated Blood Pressure Meter RH non-Automated Blood Pressure Meter with Stethoscope receive FDA 510(k) clearance?

RH non-Automated Blood Pressure Meter RH non-Automated Blood Pressure Meter with Stethoscope received FDA 510(k) clearance on 2019-05-22, under 510(k) number K190902.

Who is the listed applicant for RH non-Automated Blood Pressure Meter RH non-Automated Blood Pressure Meter with Stethoscope?

The FDA 510(k) record lists Wenzhou Renhua Instruments Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for RH non-Automated Blood Pressure Meter RH non-Automated Blood Pressure Meter with Stethoscope?

The FDA product code for RH non-Automated Blood Pressure Meter RH non-Automated Blood Pressure Meter with Stethoscope is DXQ.

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