FDA 510(k)

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

Numéro K : K230493 · 2023-11-27

Date de décision2023-11-27

Code produitGIM

Comité consultatifCH

DécisionSubstantially Equivalent

Résumé du dispositif

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.

Questions fréquentes

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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Dispositifs connexes (Code : GIM)

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Source officielle

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