FDA 510(k)

Disposable Endotracheal tube, sterile, AccuCuff

N.º K: K160694 · 2017-04-07

SolicitanteTianjin Medis Medical Device Co., Ltd.

Fecha de decisión2017-04-07

Código de productoBTR

Comité asesorAN

DecisiónSubstantially Equivalent

Resumen del dispositivo

Disposable Endotracheal tube, sterile, AccuCuff is the device name listed in this FDA 510(k) record. The listed applicant is Tianjin Medis Medical Device Co., Ltd.. It received FDA 510(k) clearance on 2017-04-07 under 510(k) number K160694. 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 Disposable Endotracheal tube, sterile, AccuCuff?

Disposable Endotracheal tube, sterile, AccuCuff is a medical device that received FDA 510(k) clearance on 2017-04-07. The listed applicant is Tianjin Medis Medical Device Co., Ltd.. The 510(k) number is K160694.

When did Disposable Endotracheal tube, sterile, AccuCuff receive FDA 510(k) clearance?

Disposable Endotracheal tube, sterile, AccuCuff received FDA 510(k) clearance on 2017-04-07, under 510(k) number K160694.

Who is the listed applicant for Disposable Endotracheal tube, sterile, AccuCuff?

The FDA 510(k) record lists Tianjin Medis Medical Device Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Disposable Endotracheal tube, sterile, AccuCuff?

The FDA product code for Disposable Endotracheal tube, sterile, AccuCuff is BTR.

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Otros registros que enlistan a Tianjin Medis Medical Device Co., Ltd. como solicitante

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Dispositivos relacionados (Código: BTR)

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Fuente oficial

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