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FDA 510(k)

Esfigmomanómetro aneróide con estetoscopio, Esfigmomanómetro aneróide

N.º K: K193259 · 2020-07-02

SolicitanteLittle Doctor Electronic (Nantong)Co.,Ltd
Fecha de decisión2020-07-02
Código de productoDXQ
Comité asesorCV
DecisiónSubstantially Equivalent

Resumen del dispositivo

Aneroid sphygmomanometer with stethoscope, Aneroid sphygmomanometer is the device name listed in this FDA 510(k) record. The listed applicant is Little Doctor Electronic (Nantong)Co.,Ltd. It received FDA 510(k) clearance on 2020-07-02 under 510(k) number K193259. The device is classified under product code DXQ. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the Aneroid sphygmomanometer with stethoscope, Aneroid sphygmomanometer?

Aneroid sphygmomanometer with stethoscope, Aneroid sphygmomanometer is a medical device that received FDA 510(k) clearance on 2020-07-02. The listed applicant is Little Doctor Electronic (Nantong)Co.,Ltd. The 510(k) number is K193259.

When did Aneroid sphygmomanometer with stethoscope, Aneroid sphygmomanometer receive FDA 510(k) clearance?

Aneroid sphygmomanometer with stethoscope, Aneroid sphygmomanometer received FDA 510(k) clearance on 2020-07-02, under 510(k) number K193259.

Who is the listed applicant for Aneroid sphygmomanometer with stethoscope, Aneroid sphygmomanometer?

The FDA 510(k) record lists Little Doctor Electronic (Nantong)Co.,Ltd as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Aneroid sphygmomanometer with stethoscope, Aneroid sphygmomanometer?

The FDA product code for Aneroid sphygmomanometer with stethoscope, Aneroid sphygmomanometer is DXQ.

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Fuente oficial

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