FDA 510(k)

Intravenous Needles for Single Use,Safety Intravenous Needles for Single Use

N.º K: K221078 · 2022-11-21

SolicitanteSichuan Prius Biotechnology Co., Ltd.

Fecha de decisión2022-11-21

Código de productoFPA

Comité asesorHO

DecisiónSubstantially Equivalent

Resumen del dispositivo

Intravenous Needles for Single Use,Safety Intravenous Needles for Single Use is the device name listed in this FDA 510(k) record. The listed applicant is Sichuan Prius Biotechnology Co., Ltd.. It received FDA 510(k) clearance on 2022-11-21 under 510(k) number K221078. 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 Intravenous Needles for Single Use,Safety Intravenous Needles for Single Use?

Intravenous Needles for Single Use,Safety Intravenous Needles for Single Use is a medical device that received FDA 510(k) clearance on 2022-11-21. The listed applicant is Sichuan Prius Biotechnology Co., Ltd.. The 510(k) number is K221078.

When did Intravenous Needles for Single Use,Safety Intravenous Needles for Single Use receive FDA 510(k) clearance?

Intravenous Needles for Single Use,Safety Intravenous Needles for Single Use received FDA 510(k) clearance on 2022-11-21, under 510(k) number K221078.

Who is the listed applicant for Intravenous Needles for Single Use,Safety Intravenous Needles for Single Use?

The FDA 510(k) record lists Sichuan Prius Biotechnology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Intravenous Needles for Single Use,Safety Intravenous Needles for Single Use?

The FDA product code for Intravenous Needles for Single Use,Safety Intravenous Needles for Single Use is FPA.

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Otros registros que enlistan a Sichuan Prius Biotechnology Co., Ltd. como solicitante

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Fuente oficial

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