FDA 510(k)

BD MiniDraw Capillary Blood Collection System with BD MiniDraw H&H Capillary Blood Collection Tube

N.º K: K230493 · 2023-11-27

SolicitanteBecton, Dickinson and Company

Fecha de decisión2023-11-27

Código de productoGIM

Comité asesorCH

DecisiónSubstantially Equivalent

Resumen del dispositivo

BD MiniDraw Capillary Blood Collection System with BD MiniDraw H&H Capillary Blood Collection Tube is the device name listed in this FDA 510(k) record. The listed applicant is Becton, Dickinson and Company. It received FDA 510(k) clearance on 2023-11-27 under 510(k) number K230493. The device is classified under product code GIM. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the BD MiniDraw Capillary Blood Collection System with BD MiniDraw H&H Capillary Blood Collection Tube?

BD MiniDraw Capillary Blood Collection System with BD MiniDraw H&H Capillary Blood Collection Tube is a medical device that received FDA 510(k) clearance on 2023-11-27. The listed applicant is Becton, Dickinson and Company. The 510(k) number is K230493.

When did BD MiniDraw Capillary Blood Collection System with BD MiniDraw H&H Capillary Blood Collection Tube receive FDA 510(k) clearance?

BD MiniDraw Capillary Blood Collection System with BD MiniDraw H&H Capillary Blood Collection Tube received FDA 510(k) clearance on 2023-11-27, under 510(k) number K230493.

Who is the listed applicant for BD MiniDraw Capillary Blood Collection System with BD MiniDraw H&H Capillary Blood Collection Tube?

The FDA 510(k) record lists Becton, Dickinson and Company as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BD MiniDraw Capillary Blood Collection System with BD MiniDraw H&H Capillary Blood Collection Tube?

The FDA product code for BD MiniDraw Capillary Blood Collection System with BD MiniDraw H&H Capillary Blood Collection Tube is GIM.

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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.