FDA 510(k)

Oxímetro de Pulso de Tipo de Dedo

N.º K: K151024 · 2016-03-02

SolicitanteTaidoc Technology Corporation

Fecha de decisión2016-03-02

Código de productoDQA

Comité asesorCV

DecisiónSubstantially Equivalent

Resumen del dispositivo

Finger Type Pulse Oximeter is the device name listed in this FDA 510(k) record. The listed applicant is Taidoc Technology Corporation. It received FDA 510(k) clearance on 2016-03-02 under 510(k) number K151024. The device is classified under product code DQA. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the Finger Type Pulse Oximeter?

Finger Type Pulse Oximeter is a medical device that received FDA 510(k) clearance on 2016-03-02. The listed applicant is Taidoc Technology Corporation. The 510(k) number is K151024.

When did Finger Type Pulse Oximeter receive FDA 510(k) clearance?

Finger Type Pulse Oximeter received FDA 510(k) clearance on 2016-03-02, under 510(k) number K151024.

Who is the listed applicant for Finger Type Pulse Oximeter?

The FDA 510(k) record lists Taidoc Technology Corporation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Finger Type Pulse Oximeter?

The FDA product code for Finger Type Pulse Oximeter is DQA.

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Dispositivos relacionados (Código: DQA)

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Fuente oficial

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