FDA 510(k)

VACUETTE EVOPROTECT Safety Blood Collection / Infusion Set

N.º K: K173757 · 2018-04-19

Fecha de decisión2018-04-19

Código de productoFMI

Comité asesorHO

DecisiónSubstantially Equivalent

Resumen del dispositivo

VACUETTE EVOPROTECT Safety Blood Collection / Infusion Set is the device name listed in this FDA 510(k) record. The listed applicant is Greiner Bio-One Na, Inc.. It received FDA 510(k) clearance on 2018-04-19 under 510(k) number K173757. The device is classified under product code FMI. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the VACUETTE EVOPROTECT Safety Blood Collection / Infusion Set?

VACUETTE EVOPROTECT Safety Blood Collection / Infusion Set is a medical device that received FDA 510(k) clearance on 2018-04-19. The listed applicant is Greiner Bio-One Na, Inc.. The 510(k) number is K173757.

When did VACUETTE EVOPROTECT Safety Blood Collection / Infusion Set receive FDA 510(k) clearance?

VACUETTE EVOPROTECT Safety Blood Collection / Infusion Set received FDA 510(k) clearance on 2018-04-19, under 510(k) number K173757.

Who is the listed applicant for VACUETTE EVOPROTECT Safety Blood Collection / Infusion Set?

The FDA 510(k) record lists Greiner Bio-One Na, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VACUETTE EVOPROTECT Safety Blood Collection / Infusion Set?

The FDA product code for VACUETTE EVOPROTECT Safety Blood Collection / Infusion Set is FMI.

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Dispositivos relacionados (Código: FMI)

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Fuente oficial

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