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FDA 510(k)

Burette-type Infusion Sets for Single Use, Disposable Infusion Sets with Precision Filters, Disposable Infusion Set

N.º K: K161898 · 2017-03-08

SolicitanteBeijing Fert Technology Co., Ltd.
Fecha de decisión2017-03-08
Código de productoFPA
Comité asesorHO
DecisiónSubstantially Equivalent

Resumen del dispositivo

Burette-type Infusion Sets for Single Use, Disposable Infusion Sets with Precision Filters, Disposable Infusion Set is the device name listed in this FDA 510(k) record. The listed applicant is Beijing Fert Technology Co., Ltd.. It received FDA 510(k) clearance on 2017-03-08 under 510(k) number K161898. The device is classified under product code FPA. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the Burette-type Infusion Sets for Single Use, Disposable Infusion Sets with Precision Filters, Disposable Infusion Set?

Burette-type Infusion Sets for Single Use, Disposable Infusion Sets with Precision Filters, Disposable Infusion Set is a medical device that received FDA 510(k) clearance on 2017-03-08. The listed applicant is Beijing Fert Technology Co., Ltd.. The 510(k) number is K161898.

When did Burette-type Infusion Sets for Single Use, Disposable Infusion Sets with Precision Filters, Disposable Infusion Set receive FDA 510(k) clearance?

Burette-type Infusion Sets for Single Use, Disposable Infusion Sets with Precision Filters, Disposable Infusion Set received FDA 510(k) clearance on 2017-03-08, under 510(k) number K161898.

Who is the listed applicant for Burette-type Infusion Sets for Single Use, Disposable Infusion Sets with Precision Filters, Disposable Infusion Set?

The FDA 510(k) record lists Beijing Fert Technology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Burette-type Infusion Sets for Single Use, Disposable Infusion Sets with Precision Filters, Disposable Infusion Set?

The FDA product code for Burette-type Infusion Sets for Single Use, Disposable Infusion Sets with Precision Filters, Disposable Infusion Set is FPA.

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Dispositivos relacionados (Código: FPA)

Los registros relacionados se emparejan automáticamente mediante nombres, códigos de producto u otros metadatos. Un emparejamiento no establece una relación clínica, científica, corporativa o regulatoria verificada; revise las fuentes oficiales enlazadas.

K254123Ecomed Disposable Administration SetsEcomed Solutions, LLCK261530iiSure Infusion SetDeka Research and DevelopmentK252543AMSafe Administration Set (BA-70075, BA-70071-D, BA-70070, BA-70071-P, BA-70072, BA-70072-F, BA-70071-DF, BA-70071-DF-120, FE01, FE04)Amsino International, Inc.K251375PuraCath Firefly Needleless Connector IT (9005)Puracath Medical, Inc.K251257nSet+ Stabilization Set [6426733]; nSet+ Stabilization Set with nSyte Needle Free Connector (NFC) [6426731]; nSyte Needle Free Connector (NFC) [6426727]Np MedicalK250325BD Alaris Pump Infusion SetCarefusion (Bd)

Fuente oficial

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Datos procedentes de la API abierta de la FDA. Para obtener la información más actualizada y autoritativa, consulte siempre el registro oficial.

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