FDA 510(k)

Yikang Endotracheal Tube

N.º K: K190213 · 2019-09-06

SolicitanteJiangxi Yikang Medical Instrument Group Co., Ltd.

Fecha de decisión2019-09-06

Código de productoBTR

Comité asesorAN

DecisiónSubstantially Equivalent

Resumen del dispositivo

Yikang Endotracheal Tube is the device name listed in this FDA 510(k) record. The listed applicant is Jiangxi Yikang Medical Instrument Group Co., Ltd.. It received FDA 510(k) clearance on 2019-09-06 under 510(k) number K190213. The device is classified under product code BTR. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the Yikang Endotracheal Tube?

Yikang Endotracheal Tube is a medical device that received FDA 510(k) clearance on 2019-09-06. The listed applicant is Jiangxi Yikang Medical Instrument Group Co., Ltd.. The 510(k) number is K190213.

When did Yikang Endotracheal Tube receive FDA 510(k) clearance?

Yikang Endotracheal Tube received FDA 510(k) clearance on 2019-09-06, under 510(k) number K190213.

Who is the listed applicant for Yikang Endotracheal Tube?

The FDA 510(k) record lists Jiangxi Yikang Medical Instrument Group Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Yikang Endotracheal Tube?

The FDA product code for Yikang Endotracheal Tube is BTR.

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Dispositivos relacionados (Código: BTR)

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